Memphis, TN - Fixed Asset Staff Accountant

Job Description:

• All Candidates should be able to start fairly quickly (2 weeks or less)
• Assignment is scheduled to last roughly fourteen (14) months.  Extensions past this time are possible and will be driven by performance and business need
• All work will be performed in Memphis, no remote work
• Work Schedule is listed as 40 hours
• Some OT may be required at peaked times but will be paid
• Pharmaceutical Experience is not required but would be a plus

REQUIREMENTS:

• Pharmaceutical Experience is not required but would be a plus
• Process fixed asset activity, reconcile various general ledger accounts, and research and resolve discrepancies to ensure
• Accounting transactions are in compliance with Pfizer accounting policies and GAAP
• Work collaboratively with Pfizer capital and finance leaders to ensure large scale capital projects are closed and recorded timely and accurately (will require strong reconciliation, problem solving, analytical, and communication skills)
• GENX large data files and prepare monthly journal entries
• Monitor FA system functionality and perform maintenance as needed to ensure data integrity (Daily/Weekly/Monthly) impacted by external feeds and various purchasing system
• Handle capital asset policy and procedure inquiries and ad hoc reporting requests; provide periodic customer/site training
• Research and resolve discrepancies and technical accounting questions
• Assist FA Supervisor as needed; participate in or lead special projects that require creative and analytical skills
• Insure customer needs and relationships are fulfilled and enhanced through proactive involvement and interaction
• involvement in projects
• Develop and assist in automating data retrieval and analysis techniques
• Maintain complete and accurate standard operating procedures and support control documentation requirements (SOX)

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North Memphis, TN - Customer Service Representative

Job Description:

• Candidate should be tested for Data entry skills and scores need to be provide

REQUIREMENTS:

• Pharmaceutical Experience is not required but would be a plus
• STRONG data entry skills and possibly some knowledge of financial adjustments (debits and credits)
• 4-7 years of experienced using MS Excel
• 1-3 years of experience with financials

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Wilmington, DE - Clinical Education and Learning Partner

Job Description:

• Determine learning needs to agreed strategy to achieve current and future business needs
• Design and manage medium-sized education programs that will drive improvements in business performance Work with internal and external Knowledge Experts to achieve desired program content
• Develop contracts for each learning program and agree with Partner Leads to ensure alignment with business objectives
• Develop metrics and conduct evaluation of learning programs and use these to determine impact on business objectives
• Work with CE&L Operations to provide appropriate documentation to enable timely delivery of solutions.
• Ability to travel overseas if required

REQUIRED:

• The role is in Education and Learning and therefore the individual does not have to have a Pharmaceutical background although this would be useful. We are looking for individuals who have worked in a learning environment developing materials both for classroom training and eLearning
• University degree or equivalent
• Five + years of work experience
• Experience of Pharmaceutical Industry, preferably within Clinical (not essential)
• Proven experience as E&L professional with wide knowledge of methods
• Specialist knowledge of design, development, delivery and evaluation of education programs
• Experience of conducting learning needs analyses and post-training evaluation
• Project management skills
• Facilitation skills
• Behavior focused on AZ values

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Raritan, NJ - SAS Programmer III

Job Description:

• To provide SAS programming support for the Clinical Research Programming Department

ESSENTIAL FUNCTIONS:

• Develop and document programs to create analysis datasets summarizing key clinical trial data
• Develop and document programs and to produce tables, listings and other reports and analyses summarizing clinical trial results
• Perform and document quality control checks for programs
• Assist in testing and implementation of new and updated internally and externally developed software as well as new SAS releases

OTHER RESPONSIBILITIES / DETAILED DUTIES:

• Participate in the development and review of study-specific procedures; participate in clinical project team meetings as required
• Assist with the development of case report forms
  
• This is not an exhaustive, comprehensive listing of job functions
• May perform other duties as assigned

PRINCIPAL RELATIONSHIPS:

• Contacts Inside the Company
• Clinical Research Programming
• Education: Bachelor’s degree or equivalent in computer science, mathematics or other scientific field (or equivalent theoretical/technical depth)

REQUIREMENTS:

• Minimum of 5 years of experience programming and analyzing scientific data in a pharmaceutical / clinical trial environment
• Expertise in SAS programming language
• Experience working in a PC SAS environment
• Must have good organization and written and oral communication skills

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Collegeville, PA - Contract Processor/Master and Agreement Data Management

Job Description:

• Participation in the data management program to ensure the quality of master and agreement data
• This involves analysis of the data and resolution by the user or self, as needed
• Reading and interpreting contracts that are sent to the Agreement Management Center, performing a quality check of the data that was entered by the user into the Agreement Management System (AMS), a central repository of executed agreements
• Resolving issues, if any, via interactions with the end users and processing the contract so that it is uploaded into the system
• Client contact for resolution of contract processing or data quality issues related to agreement or master data
• Entry and/or editing of master data for the AMS
• Evaluation and partial entry of agreement metadata that will be imported from key systems into AMS

REQUIREMENTS:

• Understanding of legal contracts
• Advanced experience using Excel
• Experience using web based systems
• Good interpersonal and client management skills – both verbal and written
• Experience with data analysis and issue resolution
• BA/BS degree required
• Paralegal experience is a plus

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Madison, NJ - Labeling Operations

With supervision, manages US Claims and Copy Clearance Committee (CCC) for assigned products / projects including:

• Managing US claims and CCC process for assigned products
• Facilitating CCC meetings including: receiving and screening agenda requests to ensure appropriateness/completeness for CCC, generating agenda, tracking action items, and offering input based on claims knowledge
• Participating in Labeling Implementation Teams (LITs) for assigned products to ensure claims deliverables are completed on target
• Ensuring claims for assigned products/projects are entered into the Consumer Claims Manager (CCM) and routed for approval
• Monitoring activity to ensure work is completed on target

REQUIREMENTS:

• BA/BS required
• Previous pharmaceutical experience required - reviewing promotional labeling information
• Candidate must have strong written and verbal communication skills

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Bridgewater, NJ - Clinical SAS Programmer

 Job Description:

• Provide statistical programming expertise (preferably in SAS) in the production of analyses, tabulations, graphics, and listings from clinical trial data
• Key responsibilities and skills include, but are not limited to, the following:  Contribute to the preparation of analysis data specifications
• Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clinical, statistical reports and other similar reports
• Contribute to the integrated clinical/statistical report and other similar documents
• Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming and reporting Perform quality assurance procedures on work performed by others
• Develop, test, validate, document, maintain and execute software and/or systems using the currently endorsed tools or support of production activities
• Assist in the integration of data from remote entry sites, contract organizations and co-licensing partners to the central database

REQUIREMENTS:

• BA, BS or MS in Mathematics, computer science or Statistics
• Three years of hands-on SAS programming experience in pharmaceutical industry
• Understands the basic skills and goals of reporting clinical data
• Writing knowledge of SAS; SQL and UNIX
• Proven ability to organize workload and priorities and complete tasks on time
• Demonstrated ability to work effectively in a team environment
• Strong interpersonal skills and ability to communicate effectively
• Ability to identify and solve technical problems

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Raritan, NJ - Microbiologist I

Job Description:

• Performs microbiological testing (to include test method development, if necessary) in support of external operating company request
• Performs microbiological testing (to include test method development, if necessary) in support of internal sterilization processes or projects
• Perform lab investigations and provide solutions to problems identified; implement improvements
• Develop, write and revise internal department procedures; generate study protocols and complete reports
• Learn new laboratory technologies

REQUIREMENTS:

• Microbiology jobs would be included in this function. 0-3 years related experience
• Experienced performing microbiological testing (to include test method development, if necessary) in support of external operating company request
• Experienced performing microbiological testing (to include test method development, if necessary) in support of internal sterilization processes or projects
• Experienced performing lab investigations and provide solutions to problems identified; implement improvements
• Experienced developing, writing and revising internal department procedures; generating study protocols and completing reports

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Fort Washington, PA - Buyer

Job Description:

• Procures materials from suppliers at the lowest cost consistent with considerations of quality, reliability of source and urgency of need
• Studies market trends, interviews vendors and recommends sources of supply
• Analyzes quotations received, selects or recommends suppliers and schedules deliveries
• Supervises preparation of orders and follows up to expedite delivery and shipment
• Develops and maintains necessary records and reports

REQUIREMENTS:

• 3 years of experience
• Experienced procuring materials from suppliers at the lowest cost consistent with considerations of quality, reliability of source and urgency of need
• Experienced studying market trends, interviewing vendors and recommending sources of supply
• Experienced analyzing quotations received, selecting or recommending suppliers and schedules deliveries
• Experienced supervising preparation of orders and following up to expedite delivery and shipment
• Experienced developing and maintaining necessary records and reports

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Warren, NJ - Principal Technician

Job Description:

• Principal Technicians in engineering or the physical sciences (e.g. chemistry) are sought to join a Research and Development team focusing on the testing of medical devices
• These technicians will be trained to use devices, such as drug-eluting stents, in bench top models simulating the clinical use of these systems and make critical performance observations
• They will use analytical instruments to determine if the devices remained intact after testing
• Also, they will set-up, maintain, and conduct baseline performance measurements on commercial and custom systems designed to fatigue the samples in order to evaluate their long-term durability

REQUIREMENTS:

• Responsible for the timely and correct execution of required tasks or tests
• Records all information obtained in experiments according to established procedure
• Operates laboratory equipment, and ensures its proper operation and maintenance; operates hands-on analytical and spectroscopic (or other types of measurement) instruments
• Experience with particulate testing using microscopy or light obscuration is desired
• Experience with pneumatic and electronic control systems is a plus
• Practices company safety and quality policies and procedures; actively requires conformance
• Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety, and Environmental compliance
• Completes required company/departmental training or equivalent in timely manner
• Initial training will be held at a remote location, ability to travel to the remote site for up to 1 month is required
• A minimum of an Associate’s Degree and 7-10 years of experience
• Experience with particulate testing using microscopy or light obscuration is desired
• Experience with pneumatic and electronic control systems is a plus
• Practices company safety and quality policies and procedures; actively requires conformance
• Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety, and Environmental compliance
• Completes required company/departmental training or equivalent in timely manner

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Athens, GA - Chemist I

Job Description:

• This position’s key function is the analytical support of Chemistry Services
• Occupants of this position will be responsible for developing new analytical methods in conjunction with process development research and product transfers
• The responsibilities include analysis of routine research samples according to existing, approved methods and newly developed, unofficial, analytical methods
• New and approved methods are transferred to the Quality Control laboratory in adherence with all regulatory and safety guidelines, including current Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP) requirements
• Maintain all of the analytical methods used to test and release product in a validated or qualified state
• Develops research proposals to provide a technically and economically sound basis for developing and evaluating new or improved products, processes, and analytical and physical testing techniques
• Performs qualitative and quantitative chemical analysis of raw materials
• Assists with special projects by supporting the development of new test methods or performing investigative test analyses as required
• Assists in projects including the validation of test methods and transfer of new products/processes/test methods

REQUIREMENTS:

• B.S. in Chemistry or related science
• Experience in instrumental and wet chemical techniques required (could be from training program); knowledge of chemical manufacturing and GMP/GLP regulations preferred

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Collegeville, PA - Records Management

Job Description:

• The assignments are estimated to last for 6-9 months
• Selected candidates will be reviewing HR records (employee files) for completeness, as well as filing them.  Some tracking in Excel will also be required
• These records will come to the department boxed, so some lifting is involved (10-20% of time)
• The filled boxes weigh ~25-30 lbs., but files may first be removed from the boxes prior to lifting
• Candidates must be able to deal with highly sensitive information, and HR background is being requested, so that they have a familiarity with the appearance of personnel files (e.g., I-9 forms)
• A degree is not required, but welcome

REQUIREMENTS:

• Some tracking in Excel will also be required
• These records will come to the department boxed, so some lifting is involved (10-20% of time)
• Candidates must be able to deal with highly sensitive information, and HR background is being requested, so that they have a familiarity with the appearance of personnel files (e.g., I-9 forms)
• A degree is not required, but welcome

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Bridgewater, NJ - Oracle Clinical & OC0RDC 2nd & 3rd Level Support

Job Description:

• Seeking a candidate with experience supporting clinical applications
• This is not a Developer position
• This is an intermediate level position
• This person will be supporting users and troubleshooting Oracle Clinical and associated applications
• The candidate should be able to work in a large team, take directions from multiple management resources
• The person should be able to handle conflicting priorities with best judgments and professionalism, and will work on multiple systems support
• The work demands availability for the candidate to be present on-site (Bridgewater) at the hours of 9 am to 6 pm, Monday through Friday (except non-business days), with occasional though rare, after hours or weekends work, as necessary

REQUIREMENTS:

• Must have a BS degree in Computer Science or Health Sciences
• Broad knowledge of Windows OS, Microsoft Office Suite applications, NT file systems, UNIX, and Citrix technology
• Three year customer support experience in Oracle Clinical (OC) and associated applications for Clinical Data Management (CDM)
• Good knowledge in OC system. (OC parameter configurations/modifications and OC data structure related issues)
• Good understanding of CDM processes such as Discrepancy Management, SAE/AE, and Coding
• Good knowledge in regulatory area and clinical development guidelines

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King of Prussia / Radnor, PA - Scientist II

Job Description:

• Accountable for the execution of cellular and molecular-based experiments for the identification and evaluation of genomic-based predictive response biomarkers for specific compounds in the Oncology pipeline
• Collaborate with cross-functional groups including internal Oncology Research and Bioinformatics personnel Generate technical reports, manuscripts and present data at internal meetings
• Assist with routine laboratory management issues

ESSENTIAL FUNCTIONS:

• Required to design and execute cellular- and molecular-based assays for the identification and validation of predictive response biomarkers
• PCR / RFLP analysis
• Taqman real-time PCR / analysis
• Western blot analysis
• RNA/DNA/miRNA isolation/ analysis
• Cell culture
• Cellular assays when needed
• Analyze public and internal genomic datasets in collaboration with Bioinformatics personnel
• Generate technical reports, manuscripts and present data at internal meetings

OTHER RESPONSIBILITIES / DETAILED DUTIES:

• Responsible for the conduct, analysis and reporting of data in accordance with requirements set forth by the department
• Ensure maintenance of detailed documentation of assay development methods and performance; record experimental data and accurate and highly organized laboratory notebooks
• Represent biomarker team at therapeutic working group meetings, as required.
• Assist with routine management of the Biomarker laboratory

REQUIREMENTS:

• Experienced in designing and executing cellular- and molecular-based assays for the identification and validation of predictive response biomarkers
• PCR / RFLP analysis
• Taqman real-time PCR / analysis
• Western blot analysis
• RNA/DNA/miRNA isolation/ analysis
• Cell culture
• Cellular assays when needed
• Experienced analyzing public and internal genomic datasets in collaboration with Bioinformatics personnel
• Experienced generating technical reports, manuscripts and present data at internal meetings

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Bridgewater, NJ - Book In Associate

Job Description:

• Enter applicable information into the global safety database for initial or follow up cases received via paper, fax or email
• Book-in, quality check and initially assess cases from suppliers sending cases to DSS via paper, email or fax Accept E2B cases received through the Argus Electronic Submissions Module (ESM) from European Health Authorities on behalf of the company’s Country Offices that are not online with Argus and other submitters as necessary Monitor electronic mailboxes and Argus ESM to ensure timely acceptance of Adverse Event (AE) Reports Perform data entry into databases, as needed
• Ensure proper coding of events and drugs for cases to ensure correct forwarding to the relevant Therapeutic Area Teams and Licensing Group
• Upload AE reports to the Drop in Data Entry II application on behalf of country offices cannot on their own

REQUIREMENTS:

• 1-3 years of Document Scanning Experience – desired
• BA degree REQUIRED for this role
• Experienced entering applicable information into the global safety database for initial or follow up cases received via paper, fax or email
• Experienced with Book-in, quality check and initially assess cases from suppliers sending cases to DSS via paper, email or fax
• Experienced ensuring proper coding of events and drugs for cases to ensure correct forwarding to the relevant Therapeutic Area Teams and Licensing Group

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Durham, NC - Biomechanical Integration Specialist

Job Description:

• Ensure optimal operations of specialized ARC R&D equipment:
• Perform preventative maintenance, new installations, troubleshoot and complete repairs as necessary
• Most of the work will be supporting incubator & hatcher operations (70%)
• Additional equipment (10%) will include animal housing & laboratory equipment
• Use expertise for troubleshooting, root cause analysis, commissioning of equipment and to anticipate possible equipment problems
• Validate to commission new equipment, decommission obsolete or faulty equipment
• Use expertise to research, recommend and implement upgrades or modifications based on needs
• Perform basic and at times complex repairs, referring to vendors when needed
• Lead projects & provide timely written and oral status/progress updates
• Ensure equipment projects (in particular incubator / hatchers) are completed in a timely manner with minimal disruptions to R&D projects
• Maintain, routinely monitor, calibrate and troubleshoot remote hatchery/vivarium monitoring system adjusting as needed
• Monitor daily and respond to alarms (24 hours)
• Use expertise to research, recommend and implement upgrades or modifications
• Help develop and manage hatchery & vivarium maintenance budget
• Ensure spare parts & supplies to ensure optimal operations
• Ensure quick turn-around, minimize down time and prevent disruption of R&D activities including those that may be required for USDA registration
• Create, record, calculate, and maintain detailed records, calibration of incubators, hatchers, cages, scales and microscopes parameters in accordance with the company’s QA policies
• Identify, develop and revise SOPs for operations as needed
• Interact, manage and coordinate vendors or internal service groups to ensure services, repairs and new equipment installation meets needs, within timelines at high quality
• Obtain, evaluate proposals and provide recommendations on appropriate course of action
• Provide information, expertise, and product support including EPH training and other functional areas in small scale incubation/hatchery/grow-out equipment maintenance & management
• Schedule, plan, communicate & maintain accurate and thorough documentation of equipment calibration, maintenance, repairs and changes performed as well as progress
• Maintain, schedule vehicles for internal use
• Provide assistance and participate in interpreting experimental, troubleshooting and inspection results and prepare reports
• Drive corrective action as appropriate
• Schedule & work with functional area leaders to ensure equipment set up & operations are optimal with no negative impact to R& D studies
• Ensure compliance with company (QA), local, state, and federal regulations such as safety, animal welfare (IACUC, AAALAC), and environmental regulations
• Prepare reports and respond to audits as needed
• Train back-up personnel on critical systems and routine checks
• Participation in hatchery and animal husbandry activities will be required (20%)

REQUIREMENTS:

• Two year degree in a mechanical or electrical technology field required with 7-10 years of experience or a 4 year degree with 1-3 years of experience
• Agricultural equipment management, hatchery or animal/poultry equipment repair experience highly desirable
• Knowledge of electrical, plumbing, vendor management, and general equipment repair & maintenance required
• Excellent interpersonal skills
• Excellent written and oral communication skills (proficient in Word & Excel)
• Established project management skills
• Required 24 hour on call for equipment alarms. Handle after-hours weekday, weekend, and holiday incubator/hatchery alarm condition
• May not own birds or poultry

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Groton, CT - Financial Analyst

Job Description:

• Provides financial analytical support to the eTMF Technical Team for the budgeting and forecasting processes for a major program, as well as reporting actual financial results on a monthly basis
• Offers professional judgment on financial matters and processes monthly transactions to the general ledger
• Supports activities relating to internal corporate accounting and finance systems
• Ensures compliance with accounting standards and internal policies

REQUIREMENTS:

• ARIBA: Required 4-7 Years Intermediate
• Business Objects: Required 4-7 Years Intermediate
• Cognos: Required 4-7 Years Intermediate
• MS Excel: Required 4-7 Years Intermediate
• MS Word: Required 4-7 Years Intermediate
• PeopleSoft: Required 4-7 Years Intermediate
• Knowledge of Pfizer Corporate accounting standards and internal policies
• Experienced with Computron
• Experienced with WTPS
• Knowledge of Corporate Accounting and Finance Systems (identified in Job Description)

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New Brunswick, NJ - Sourcer

Job Description:

• We are seeking Contract Talent Identification Consultants to proactively identify and recruit top talent in a highly competitive employment marketplace
• In this role you will be responsible for the delivery of high quality professional and executive level candidates by utilizing strategic sourcing methodologies, business intelligence, internal and external networks, professional organizations, branding initiatives, and technology tools in support of strategic business objectives and in partnership with Recruiters and Hiring managers within the Family of Companies
• The Contract Identification Consultant is focused on providing and managing the full spectrum of recruitment sourcing services for the family of companies that make up the company
• This position will be responsible for driving compliance in the talent acquisition process across all stakeholder groups - hiring managers, recruiters, HR, candidates, and the Talent Acquisition Group
• Through excellent service delivery and expert consultation, gains the trust and confidence of candidates, recruiters, and hiring managers is an integral part of the recruiting team
• The incumbent will ensure that the company is represented in the most accurate and appropriate way to all candidates, and personally drives the highest standards of ethical behavior for all involved in the recruiting process
• This person will also maintain accurate, updated and compliant information in employment management systems
• In addition, will exercise appropriate discretion in the expenditure of company resources related to the recruiting/sourcing process, ensuring the appropriate risk/benefit and/or return on investment is provided for expenditures

REQUIREMENTS:

• A minimum of Bachelor's degree is required
• At least 5 years of documented success in a recruiting role either in a corporate or agency setting is required
• Total experience can also include some years of related experience in recruiting or sourcing (i.e. recruiting responsibility in an HR generalist role)
• A demonstrated capability in high-volume recruiting for a wide variety of exempt positions within Marketing, R&D, and/or Finance is highly desired
• Candidate should have strong analytical skills, demonstrated interpersonal skills, and competence working both individually and as a team member
• Candidate should demonstrate the ability to multitask, work in a fast-paced environment, and work with highly confidential information
• Preferences include documented success in the recruiting industry, developed passive recruiting skills, i.e. Cold Calling, established functional network, training in behavioral interviewing assessment, honed candidate management skills, AIRS or related certification, experience in niche or function
• Experience with Taleo or other similar Applicant Tracking Systems is required

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Skillman, NJ - Scientist I

Job Description:

• Uses the principles and theories of science and mathematics to solve problems in R&D and to help invent and improve products-processes
• Performs qualitative and quantitative chemical analysis of raw materials
• Coordinates testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow
• Functions as a team member in the QA Chemical Laboratories to provide timely test analysis information on the status of conformance to requirements
• Investigates testing abnormalities and implements corrective action
• Assists with determination of root causes of non-conformances and recommends corrective actions
• Audits documentation, device history records, and test methods for compliance
• Assists with special projects by supporting the development of new test methods of performing investigative test analyses as required
• Assists in projects including the validation of test methods and transfer of new products-processes-test methods

REQUIREMENTS:

• 0-3 years of experience
• Experienced using the principles and theories of science and mathematics to solve problems in R&D and to help invent and improve products-process
• Experienced performing qualitative and quantitative chemical analysis of raw materials
• Experienced coordinating testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow
• Experienced investigating testing abnormalities and implementing corrective action
• Experienced auditing documentation, device history records, and testing methods for compliance

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Somerville, NJ - Marketing Analyst I

Job Description:

• Analyze and summarize financial data and data from external and internal sources
• Gather and enter global sales forecast data into financial systems
• Download data from internal financial system to Excel Develop and distribute standard/ad hoc business reports, financial analysis, and effectiveness tracking
• Prepare comparisons with previous year results
• Manual data entry to the system

REQUIREMENTS:

• Minimum 5 years of experience and analytical/financial data background
• Experienced analyzing and summarizing financial data and data from external and internal sources
• Experienced gathering and entering global sales forecast data into financial systems
• Experienced downloading data from internal financial system into MS Excel
• Experienced developing and distributing standard/ad hoc business reports, financial analysis, and effectiveness tracking
• Experienced preparing comparisons with previous year results

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Jacksonville FL - Scientist I

Job Description:

• Uses the principles and theories of science and mathematics to solve problems in the QA Chemistry Laboratory and to help improve products-processes Performs qualitative and quantitative chemical analysis of raw materials and finished products
• Coordinates testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow
• Functions as a team member in the QA Chemical Laboratories to provide timely test analysis information on the status of conformance to requirements
• Assists with special projects by supporting the development of new test methods of performing investigative test analyses as required
• Assists in projects including the validation of test methods and transfer of new products-processes-test methods

REQUIREMENTS:

• Minimum of 1 year of HPLC experience – required
• Experienced performing qualitative and quantitative chemical analysis of raw materials and finished products
• Experienced coordinating testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow

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