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Chemist

Job Title: Chemist.
Job ID: 7195
Location: North Haven CT 06473
Duration: 18 months
Shift: 2nd shift (3p-11p)

Summary Of Position
The individual will be responsible for providing analytical support to the PDBMF Quality Control Department. The individual will be responsible to follow established procedures and protocols to conduct various independent and team driven laboratory experiments. This individual will be responsible for the analysis of samples to determine their chemical and physical properties. Assist with the day-to-day maintenance of an orderly QC laboratory such as safety, Instrument calibration, data review, technician training.

Scope Of Duties/Job Description:
Maintain a safe working environment that is in compliance with all applicable EH&S regulations.
Ensure Health and Safety is the number one goal by following policies, processes, and acting in a safe manner at all times.
Perform analysis of samples following prescribed procedures, with the ability to solve minor problems.
Analyze raw material, finished product, in-process samples, including research oriented samples.
Responsible for conducting investigations on aberrant results.
Participate in collaborative studies and may serve as a team leader for a project or study.
Training other Chemists to properly perform laboratory procedures.
Recommend changes to test procedures to reduce variability and/or improve efficiency.
Assist in the day to day maintenance of the QC laboratory
Calibrate and maintain analytical instrumentation.
Complete all paperwork associated with the analyses of incoming material in a timely fashion.
Ensure that all work meets applicable specifications.
Management waste generated as a result of analytical procedures.
Work under minimal supervision.
Perform training and other aspects as directed by Lab Supervisor.
Review and update applicable laboratory SOPs as necessary.
Manage applicable staff and programs within the PDBMF Polymer Laboratory
Assist in the recruitment of staff members, conduct performance appraisals, and fulfill other managerial responsibilities as required
Provide direction, subject matter expertise, training material, mentoring to the PDBMF Quality Team.
Organize and direct investigations to review findings and advise on study direction, as needed
Provide input and support for Laboratory Investigation activities
Coordinate closely with cross-functional leaders to ensure optimal alignment of site goals.
Ensure appropriate resources are maintained for the various projects assigned to their area
Provide management level representation during audits
Regularly interact with senior management and prepare periodic reports as required for management review
Perform as project manager for some projects
Perform other clinical duties when requested

Education And/Or Experience
Bachelors degree or higher in chemistry or related field or a minimum of 3 year experience in a cGMP Regulated polymer chemistry laboratory is preferred.

Quality Control Chemist II will be responsible for the testing, results documentation and data review of any of the following: raw materials, in-process, finished product, calibrations, stability, technical service samples or projects within the QC Chemistry Laboratory, in a manner consistent with established standards.
Independently perform core techniques or methods as assigned for testing on raw materials, in-process, release, stability, and engineering or research samples as assigned.
Perform testing that has a higher level of difficulty compared to other testing methods.
Ensure that the calibration of critical laboratory equipment is current before use.
Quality Control Chemist II will perform analytical testing of products following analytical methodology.
Read and interpret analytical methodology.
Perform method development and validation. Follow cGMP, cGLP, and USP and FDA requirements.
Operate analytical instrumentation.
Ability to perform calibrations and troubleshoot instrumentation as needed.
Write SOP s for new methods as needed.
Ensure testing is performed accurately and in compliance with GLP, GMP, USP, SOP and other approved test methods.
Follow all company policies, standard operating procedures, work instructions, methods and analysts guidelines.
Record and/or review all data and document all activities in accordance with applicable guidelines, SOPs and Company policies.
Document all aspects of assignments on approved laboratory worksheets and laboratory notebook.
Draft, finalize necessary summaries and reports.

Contact Person: Manju

If you are inteterested in this position then you can reach me at 2015249600 X 9744
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