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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Good Manufacturing Practices (cGMP) and safety regulations while effectively operating manufacturing process control systems. Capable of performing analytical analysis and maintaining compliance in a team-oriented environment.
Highest-signal resume keywords
Good Manufacturing Practices (cGMP)Clean In Place (CIP) Equipment OperationSAP and/or ACSIS TransactionsBioworks CertificateDetail Oriented
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Manufacturing Process Control SystemsAnalytical AnalysisRecord KeepingBatch Production RecordsBuffer and Process Solutions PreparationSampling OperationsMechanical AptitudeBasic Math SkillsBasic Computer SkillsSafety Guidelines Knowledge
Soft Skills
Team CollaborationGood JudgmentExcellent Communication SkillsWillingness to LearnDetail Oriented
Certifications & Qualifications
High School Diploma or EquivalentBioworks Certificate Preferred
Industry Keywords
Human Blood Plasma ManufacturingSafety RegulationsState and Federal Health RegulationsEnvironmental RegulationsSOPs
About the role
Key responsibilities & impact- Manufacture products derived from human blood plasma
- Follow company safety guidelines and programs
- Care for facility, equipment, systems, and product
- Perform personal hygiene and proper gowning
- Follow SOPs and complete Batch Production Records
- Complete record keeping according to current Good Manufacturing Practices
- Operate manufacturing process control systems and equipment
- Operate Clean In Place (CIP) equipment
- Perform in-process analytical analysis
- Monitor manufacturing processes
- Assist with sampling operations and harvesting intermediate products
- Prepare, set up, and transfer buffer and process solutions
- Transfer intermediate product, raw materials, and waste
- Stage plasma, intermediate paste, and raw materials
- Clean and sanitize designated manufacturing areas
- Utilize SAP and/or ACSIS transactions
- Support production supply-chain requirements
- Assist team members and supervisors with additional tasks
- Execute commissioning and validation activities for a new building
- Communicate with operators, technicians, and supervisors
- Work ethically and compliantly to manufacture safe drug products
Requirements
What you’ll need- Basic math skills
- Basic computer skills
- Mechanical aptitude
- Detail oriented
- Ability to work in a team environment and exercise good judgment
- High school diploma or equivalent
- Bioworks Certificate preferred
- Knowledge of company safety guidelines and SOPs
- Strong knowledge of current Good Manufacturing Practices (cGMP)
- Knowledge of State and Federal Health, Environment and Safety regulations
- Excellent oral and written communication skills
- Ability to work a 24/7 rotating shift schedule
- Comfortable using different computer systems for data entry
- Willingness to learn from other manufacturing team members
- Requires kneeling, climbing, squatting, standing, bending, and twisting
- Ability to lift and carry up to 50 lbs
- Ability to work at heights on platforms and ladders
- Ability to adapt to a fluid schedule during commissioning and validation
- Level II advancement typically requires a minimum of 12 months as a Technician in the respective department and a meets-expectations performance review
Benefits
Comp & perks- Equal employment opportunities and consideration consistent with applicable laws
- 12-hour day shift schedule