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Quality Control Data Reviewer

Harmans, MD

Posted: 01/19/2021 Industry: Manufacturing Technician Job Number: JN -122020-12286

Job Description

Quality Control Data Reviewer

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.
  • Title: Quality Control Data Reviewer
  • Location: Harmans, MD
  • Industry: Pharmaceutical
  • Hours: 1st shift 8-5pm
  • Salary: $36.06hr (Paid Weekly - Benefits Available)
  • Employment Type: 6 month Contract
Environment: This client manufactures thousands of pharmaceutical, biologic, consumer health and beauty products utilizing superior and innovative drug delivery technologies to improve their value to patients and consumers. Our customer believes in a Patient First culture putting patients at the center of their work to ensure the safety, reliable supply and optimal performance of our products.

Knowledge/Skills Requirements:
Receive Batch Records from other departments
Receive and organize completed Test Records
Update data trackers with Test Record results
Transcribe data to Batch Record tables
Pairing of completed Test Records with Batch Records
Order and receive supplies for groups
Execute document revisions
Provide QC data to other departments as needed
Effectively communicates updates and results
Flexibility in following unique campaign requirements that may include off-hour and weekend work
Other duties as assigned

SKILLS & TECHNICAL EXPERTISE:
Ability to produce results in a fast-paced environment to meet client deadlines under minimal supervision
Experience within the biologic, pharmaceutical, or medical device industry performing direct hands-on work in a Quality Assurance/QC function with a strong familiarity of general GMP practices
Able to work in a team setting and independently under minimum supervision
Experience with MS Excel and Word for tracking of testing.
Document writing, data interpretation, presentation, statistical analysis and trending a plus

Qualifications:
B.S. or A.S. in a Life Sciences discipline with a minimum of 1 year experience preferred
Experience working in cGMP Quality Control
Experience with Microsoft Excel and Microsoft Word
Strong attention to detail and strong organizational skills
Strong verbal communication skills with outside contract laboratories
Familiarity with Good Manufacturing Practices (cGMP s)
Have the knowledge and ability to apply basic scientific and regulatory principles utilized to solve operational, as well as routine quality tasks
Ability to succeed in a team-oriented environment under very dynamic conditions

MEASUREMENT OF PERFORMANCE:
Positive, professional attitude toward work and willingness to cooperate with co-workers and supervisors and to contribute to a project team
Dependable and can work with minimal supervision on scheduled tasks
Timeliness and accuracy in completion of projects and paperwork (quantity of work)
Contributions to projects beyond general responsibilities (quality of work)
Identification of problem areas affecting operations (knowledge/problem solving)
Offers suggestions for correcting problems and for improving operations
Exercises good judgment in dealing with operational problems
Understanding of theory, rationale behind tasks performed
Demonstrated understanding and adherence to Paragon policies, safety procedures and the cGMPs
Ability to succeed in a team-oriented environment under very dynamic conditions


EOE/ADA


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