Quality Operations Specialist II - Night Shift 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 Specialist II - Night Shift - Contract - Philadelphia, PA

Proclinical is seeking a dedicated Quality Operations Specialist II to join an established biotech. This position is crucial for maintaining compliance with current Good Manufacturing Practices (cGMPs) and facility procedures.

Primary Responsibilities:

The successful candidate will interface with various functional groups, such as Manufacturing, Quality Control, and Document Control, to identify and report events like errors, deficiencies, discrepancies, deviations, and other observations to management.

Skills & Requirements:

Bachelor's Degree in Science, Engineering, or a related technical discipline, or equivalent industry experience.
Working knowledge of Good Manufacturing Practices (cGMPs) regulations.
Ability to work in an aseptic processing environment.
Strong administrative skills, including proficiency in Microsoft Word, Excel, and PowerPoint.
Excellent attention to detail.
Knowledge of QMS systems is a plus.

The Quality Operations Specialist II's responsibilities will be:

Maintain strict adherence to Good Manufacturing Practices (cGMPs) and facility protocols.
Interface with Manufacturing, Quality Control, and Document Control to identify and report events such as errors, deficiencies, discrepancies, deviations, and other observations to management.
Review batch records and related production documentation, resolving identified issues before product disposition.
Collaborate with internal functions to address issues promptly.
Disposition incoming raw materials.
Apply quality compliance theories and principles to address issues independently.
Provide guidance on controlled documents, identifying gaps, and suggesting process improvements.
Maintain and report on Quality Metrics.
Initiate and participate in SOP revisions to improve compliance.

Compensation:

USD 30-40 per hour

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

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.

Related jobs

GMP QC Analyst

Salary

US$25 - US$30 per hour

Location:

Norton, USA

Proclinical is on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world.