Chemist II

Integrated Resources Inc.; Lancaster (Lancaster County); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading staffing firm is seeking a Quality Control Chemist for a 12+ month contract in Lancaster, PA. The role involves testing and ensuring the quality of pharmaceutical products in compliance with safety regulations. Ideal candidates will possess a BS/BA in a Science and have a minimum of 3 years experience in a GMP QC Laboratory environment, demonstrating professionalism and teamwork.

Qualifications

• Minimum 3 years GMP QC Laboratory Experience.
• Must demonstrate a positive attitude.
• Ability to work independently and as part of a team.

Responsibilities

• Provides testing and technical support in the Analytical QC Laboratory.
• Processes and tests samples of raw materials and finished products.
• Maintains compliance with cGMP's and safety regulations.

Skills

Professionalism

Ethics

Teamwork

Initiative

Communication

Education

BS or BA in a Science (Chemistry preferred)

Job description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

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.

Additional Information

Thanks & Regards,

Seema Chawhan Clinical Recruiter Integrated Resources , Inc. IT Life Sciences Allied Healthcare CRO Certified MBE | GSA - Schedule 66 I GSA - Schedule 621I

DIRECT # - 732-844-8724 |

LinkedIn: https://in.linkedin.com/in/seemachawhan Gold Seal JCAHO Certified for Health Care Staffing “INC 5 0 0 0 ’s FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)