Posted in Other 13 days ago.
Location: Oceanside, California
Innova Solutions is immediately hiring for a Manufacturing Commissioning & Qualification Technician
Position type: Full
time Contract
Duration: 10 months
Location: Oceanside, CA
As a Manufacturing Commissioning & Qualification Technician, you will:
Job Description:
Job Summary:
The Manufacturing Commissioning Qualification CQ Technician position at client is the equivalent to and is a part of the manufacturing technician job family.
This role would be equivalent to a senior or master technician position.
The Manufacturing CQ Technician is an integral member of the OSUT Oceanside Single Use Technology team in Oceanside.
The OSUT is designed to be a state-of-the-art large molecule drug substance facility which supports GMP production for phase 3 clinical trials and commercial products.
The OSUT will employ a ballroom design utilize single-use technology new analytical techniques and digital manufacturing systems to deliver a best-in-class bioprocess facility.
We are looking for individuals to support this facility who are comfortable with ambiguity have an entrepreneurial spirit within a GMP environment have demonstrated strong Pharma Technical Behaviors and have an agile mindset.
Ability to collaborate is crucial as success will be measured as a member of a team not just as an individual.
Ideal candidates would have experience in a broad range of functional roles in support of biopharmaceutical production.
The team members will work closely with the existing staff in the stainless-steel operations as well as with South San Francisco Clinical Supply Center CSC.
In this role the qualified individual will be part of the Operations Process Support and Process Engineering team that starts up the facility.
There will be one team that will support the entire process from initial cell bank thaw through bulk freeze.
Team members will support manufacturing operations upstream and downstream but will also have responsibility for technical evaluations troubleshooting and work with the project team on equipment or consumable design.
The candidate will engage with customer groups network teams and project teams to seek opportunities for collaboration proactively communicating and presenting information and offering relevant data driven information to impact decisions.
Duration and Potential Extension:
The role requires 100-time commitment at site Oceanside through the end of 2024 with potential extension based on the development and achievement of deliverables.
The high-level work outcomes are:
Process equipment installed per design.
Start-up Commissioning and Qualification activities completed on schedule.
OSUT Manufacturing Core is fully qualified up to OQ and can be released for GMP use. Deliverables and Milestones
Successful Automation SAT completion
Completion of Operation Verification
Successful Water Run for Process Equipment completion.
Successful Technical Run for Process Equipment completion
Primary Responsibilities:
Interfacing with highly automated production systems and controls in cGMP manufacturing environment
Assemble prepare and operate equipment for manufacturing operations including cell culture or purification e.g. culture growth process monitoring sampling harvesting purification formulation freeze thaw and transfer.
Performs media/buffer solution preparation operations.
Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices cGMP and Standard Operating Procedures SOP.
Troubleshoot and investigate complex problems and work with others to implement solutions.
Participates in safety assessments/reviews.
Ensures necessary operating procedures are in place prior to CQ execution on the assigned unit operations.
Ensures training materials and curriculum are developed and revised as needed.
Performs/updates risk assessments in partnership with network and Quality counterparts.
Coordinates and conducts start-up and troubleshooting activities.
Execute equipment CQ write-up and review using existing documentation and protocols.
Collaborate with the client Automation engineering team to coordinate control systems design installation and commissioning needed for the core processing systems.
Target Experience Knowledge:
Degree in Life Sciences or Engineering and 7 years' experience - Biotech certificate from approved program.
Prefer experience knowledge working with Single Use Technologies or modular.
Knowledge Skills and Abilities:
Excellent oral and written communication skills demonstrated by communicating with other functions and management regarding resolving investigations and theory.
Ability to lead department and/or cross functional meetings or project.
Comfortable working in an agile and ambiguous environment
Has demonstrated a commitment to quality.
Work Environment/Physical Demands/Safety Considerations:
Work in office manufacturing and to a lesser extent laboratory environment.
May be on feet for 4 to 5 hours a day.
Able to work a flexible schedule to meet start-up activity requirements.
Lifting up to 25lbs may be required.
May work in the clean room environment that requires gowning in the form of hospital scrubs coveralls gloves and steel toe boots be worn.
Also, no makeup or jewelry can be worn when working in the clean room environment.
May work with hazardous materials and chemicals.
Most of the time will work a standard Monday - Friday 8am - 5pm type of schedule.
There will be times where we need to work a shifted 12/12/12/4 Schedule during the technical run.
Expected to last about 6 weeks. Sometime in August/September timeframe
Qualified candidates should APPLY NOW for immediate consideration! Please hit APPLY to provide the required information, and we will be back in touch as soon as possible.
We are currently interviewing to fill this and other similar positions. If this role is not a fit for you, we do offer a referral bonus program for referrals that we successfully place with our clients, subject to program guidelines. ASK ME HOW.
Thank you!
Deeksha Gupta
Team Lead - Recruitment
(+1) 213-788-7669
Deeksha.gupta@innovasolutions.com
PAY RANGE AND BENEFITS:
Pay Range*: $48- $55 per hour
*Pay range offered to a successful candidate will be based on several factors, including the candidate's education, work experience, work location, specific job duties, certifications, etc.
Benefits: Innova Solutions offers benefits( based on eligibility) that include the following: Medical & pharmacy coverage, Dental/vision insurance, 401(k), Health saving account (HSA) and Flexible spending account (FSA), Life Insurance, Pet Insurance, Short term and Long term Disability, Accident & Critical illness coverage, Pre-paid legal & ID theft protection, Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP).
ABOUT INNOVA SOLUTIONS: Founded in 1998 and headquartered in Atlanta, Georgia, Innova Solutions employs approximately 50,000 professionals worldwide and reports an annual revenue approaching $3 Billion. Through our global delivery centres across North America, Asia, and Europe, we deliver strategic technology and business transformation solutions to our clients, enabling them to operate as leaders within their fields.
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