Chemist II

Job Title: Chemist II

Location: LANCASTER, PA
Duration: 12+ Months (Possibility of extension)
Shift: 8Am -5Pm

JOB DECRIPTION

·Provides testing and technical support in the Analytical QC Laboratory.

·Processing and testing samples of raw materials, packaging components, bulk and finished products, stability samples, process validation, and cleaning validations for Pharmaceutical Consumer, Inc. and other affiliates to guarantee that they conform to specifications and standard operating procedures (SOPs).

·Prepares diluents, solutions, reagents, etc. in accordance with approved SOPs, Component Specifications, Method Specifications, Protocols, and/or compendia to expedite laboratory testing.

·May review and/or assist in writing SOP's and laboratory investigations.

·Provide technical guidance for other less experienced Chemists and Technicians.

·Provide technical support and trouble-shooting for analytical issues and investigations.

·Complies with cGMP's and safety regulations.

·Maintains an environment of respect and teamwork with all coworkers

RESPONSIBILITIES:
(Define key accountabilities and/or activities.) Under limited supervision and in accordance with all applicable federal, state and local laws/regulations, the Companies' policies, procedures and
guidelines, this position:
Quality & Compliance:

·Ensure quality and compliance by the following actions:

·Attend GMP training on the schedule designated for this role and as appropriate for this role.

·Adhere to strict compliance with procedures applicable to my role.

·Exercise the highest level of integrity in the tasks that I perform.

·In a timely and prompt manner, identify report and seek correction for deviations noted in my workplace.

·Embrace a behavior of employee involvement and commitment to doing the job right the first time.

Laboratory Operations:

·Supports the laboratory operations by the following actions:

·Performs testing on raw materials, in-process, finished product, packaging, and stability samples utilizing instrumentation such as HPLC, GC, FTIR, Dissolution and ICP in accordance with approved SOPs, Component Specifications, Method Specifications, Protocols, and/or compendia.

·Reviews and approves laboratory data generated by other Analysts for completeness and accuracy.

·Assist with support of laboratory investigations as needed.

·Reviews and/or assists in providing input and/or writing SOP's.

·Perform instrument calibrations and assist in qualifications as trained.

·Identifies and implements opportunities to improve laboratory efficiencies.

·Assist with the training of other Analysts on specific instruments or techniques.

·Participates in meetings outside of the department as determined by a Supervisor.

·Performs other related duties as required.

EDUCATION:

·BS or BA in a Science (Chemistry preferred) or Technical field.

EXPERIENCE:

·Minimum 3 years GMP QC Laboratory Experience.

·Knowledge, Skills and Abilities:

·Must be professional and ethical in all activities and relations.

·Must demonstrate through example and maintain a positive attitude.

·Must exhibit the initiative to take on individual projects, eliminate roadblocks and see them through to completion.

·Capable of working both independently and as a team member.

·Ability to work and communicate well with personnel in different departments and at various levels of responsibility.