Work Schedule
First Shift (Days)Environmental Conditions
OfficeJob Description
Key Responsibilities:
Review complex or high-risk production records for GMP compliance.
Collaborate with cross-functional teams (Manufacturing, QC) to ensure timely batch release.
Provide guidance and on-the-job training for new technicians.
Assist in preparation for regulatory and client audits.
Lead initiatives to streamline batch review and electronic systems.
Follows all job-related safety and other training requirements.
Education
High School diploma / equivalent minimally required.
Associates degree or higher in Science or Technology is preferred
Experience
Required: Minimum of 2 years of work experience in QA or QC or related field
Required: Experience in a cGMP environment
Equivalent combinations of education, training, and meaningful work experience may be considered
Knowledge, Skills, Abilities
Strong understanding of cGMP and batch documentation flow.
Good verbal/written communication skills to partner with production teams.
Excels in a team environment.
Basic math skills.
Attention to detail while maintaining quality.
Ability to follow SOPs.
Physical Requirements/Work Environment
Use Personal Protective Equipment (PPE) and understand chemical hygiene.
Infrequently lift and manipulate up to 50 pounds max unassisted.
Stand and move about including reaching, bending, stooping, grasping.
Use hand tools and equipment including forceful gripping, grasping, pushing and pulling.
Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 10-35 pounds.
Job details are sourced from the employer's original posting.
Open job postingAbout the company
Patheon Manufacturing Services LLC is a contract development and manufacturing organization (CDMO) providing pharmaceutical and biopharmaceutical services.