QA Specialist - II job in Oceanside, 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...

Proclinical is currently recruiting for a Quality Assurance Specialist - II position with an international biopharmaceutical company located in Oceanside, CA. Successful candidate will participate in developing Standard Operating Procedures to ensure quality objectives are met.

Job Responsibilities:

Performs a wide variety of activities to ensure compliance with applicable regulatory requirements.
Maintains programs and processes to ensure high quality products and compliance with current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs).
Perform Quality Assurance related production and production related activities

Issuance of production records, procedures and labels
Ensure timely assessment and closure of discrepancies, Deviations and Change Controls requests
Ensure timely assessment and closure of Laboratory Investigations
Ensure timely assessment and closure of batch and material hold events
Communicate lot disposition pending issues to Management
Oversee the packaging and shipping process; authorize shipment.

Review and disposition disposable raw materials and components for GMP use
Provide on-the-floor QA oversight and support to ensure compliance to GMP throughout the area
Perform walk-throughs and process observations
Ensure products are manufactured in compliance with regulatory and GMP guidelines.
Escalate issues that may adversely impact timely release of product
Identify compliance risks and escalate the issues to appropriate levels of management for resolution
Generate and update procedures and forms.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Brendan Thalheimer at (+1) 215-531-5299 or upload your resume on our website - www.proclinical.com.

A full job description is available on request.

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.

#LI-BT1
#Compliance/Quality

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.