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Associate Manufacturing Process Technician - (JP11426)
Thousand Oaks, CA · Biotech/PharmaceuticalJob Title: Associate Manufacturing Process Technician - (JP11426)
Location: Thousand Oaks, CA. 91320
Business Unit: Clinical Operations Administration
Employment Type: Contract
Duration: 2+ years (with possible extensions and/or conversion to permanent).
Pay Rate: $18.00 – $22.00 per hour
Posting Date: 5/1/21
Notes: Only qualified candidates need apply. Onsite in Thousand Oaks, CA.
3 Key Consulting is recruiting an Associate Manufacturing Process Technician for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Onsite in Thousand Oaks, CA. Standard work hours. The candidate will work in a highly collaborative team environment and be responsible for both moderately-complex to complex nGMP and GMP manufacturing activities to support of our early phase clinical pipeline of synthetic drug products. Activities may include:
Top Must Have Skill Sets:
Day to Day Responsibilities:
Why is the Position Open?
Supplement additional workload on team
Employee Value Proposition:
Career growth, opportunity
Red Flags:
No prior experience in the pharmaceutical industry.
Interview Process:
2 phone interviews. One with the hiring manager and another with team members.
We invite qualified candidates to send your resume to . If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
Location: Thousand Oaks, CA. 91320
Business Unit: Clinical Operations Administration
Employment Type: Contract
Duration: 2+ years (with possible extensions and/or conversion to permanent).
Pay Rate: $18.00 – $22.00 per hour
Posting Date: 5/1/21
Notes: Only qualified candidates need apply. Onsite in Thousand Oaks, CA.
3 Key Consulting is recruiting an Associate Manufacturing Process Technician for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Onsite in Thousand Oaks, CA. Standard work hours. The candidate will work in a highly collaborative team environment and be responsible for both moderately-complex to complex nGMP and GMP manufacturing activities to support of our early phase clinical pipeline of synthetic drug products. Activities may include:
- Hands-on cleaning, sanitization, and setup of processing equipment and process rooms
- Support in manufacturing process readiness activities
- Assist in the review of facility and equipment documentation (equipment/room logbooks)
- Maintenance of Raw Materials & Consumables Inventory
- Supporting the day to day operational needs of the facility
Top Must Have Skill Sets:
- Associate’s degree in science/pharmaceutical science-related area
- Ability to adhere to current Good Manufacturing Practices cGMPs and follow Standard Operating Procedures SOPs.
- Understanding of typical unit operations for the manufacture of synthetics drug product (i.e. granulation, roller compaction, drying, milling, blending, compression, encapsulation and film coating)
- Strong technical skills to support problem solving exercises.
- Strong interpersonal skills and a proactive leadership mindset
- Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Day to Day Responsibilities:
- Perform cleaning, sanitization, and setup of processing equipment and process rooms
- Support in manufacturing process readiness activities
- Supporting the day to day operational needs of the facility
- Identify, recommend, and implement improvements related to routine functions
- PPE familiarity and ability to use a PAPR
- Ability to work with Microsoft Word, Excel, and PowerPoint
- Excellent verbal and written communication skills
- The candidate will collaborate in multi-disciplinary teams with Process Development scientists, engineers, EH&S, Quality, F&E, maintenance, and other supporting functions.
Why is the Position Open?
Supplement additional workload on team
Employee Value Proposition:
Career growth, opportunity
Red Flags:
No prior experience in the pharmaceutical industry.
Interview Process:
2 phone interviews. One with the hiring manager and another with team members.
We invite qualified candidates to send your resume to . If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
Regards,
3KC Talent Acquisition Team