Quality Operations Associate job in Philadelphia, USA

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

Job type: Contract

Discipline: Good Manufacturing Practice (GMP)

Location: United States

This vacancy has now expired. Please see similar roles below...

Quality Operations Associate- Contract - Philadelphia, PA

Proclinical is seeking a Quality Operations Associate who will play a crucial role in ensuring compliance with cGMPs and facility procedures.

Primary Responsibilities:

The successful candidate will collaborate with various functional groups, such as Manufacturing, Quality Control, and Document Control, to identify and report any events such as errors, deficiencies, discrepancies, deviations, and other observations. This role involves reviewing batch records and related production documentation, ensuring all identified issues are resolved before product disposition. The Quality Operations Associate will also be responsible for the disposition of incoming raw materials and maintaining Quality Metrics.

Skills & Requirements:

Bachelor's Degree in Science, Engineering, or a related technical discipline or equivalent industry experience.
At least 1- 3 years' experience in a regulated industry.
Knowledge of cGMP regulations.
Ability to work in an aseptic processing environment.
Strong administrative skills including use of Microsoft Word, Excel, and PowerPoint.
Attention to detail.
Knowledge of QMS systems is a plus.

The Quality Operations Associate's responsibilities will be:

Ensure compliance to cGMPs and facility procedures.
Collaborate with functional groups to identify and report any events.
Review batch records and related production documentation.
Resolve all identified issues before product disposition.
Disposition incoming raw materials.
Maintain and report on Quality Metrics.
Initiate and participate in standard operating procedure (SOP) revisions.
Perform other tasks as assigned.

Compensation: USD 35 - 38 per hour

If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at s.briggs

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

INDCQA

Related jobs

Formulation Scientist (Lab worker)

Salary

Highly Competitive

Location:

Basel, Switzerland

Shape the future of oral drug delivery-join a leading pharma team as a Formulation Scientist bridging innovation and GMP production.

Emile De Beer

Apply

QC Analyst (junior)

Salary

Highly Competitive

Location:

Neuchâtel, Switzerland

Step into the heart of Swiss pharma as a Junior QC Analyst-where your precision, French fluency, and GMP expertise ensure quality from sample to solution.