Biopharmaceutical Manufacturing Associate

Job Title: Senior Process Technician

Location: Andover, MA

Workplace Type: Onsite role

Work Schedule: Monday to Friday

Duration: 8 months, W2 Contract

No of roles : 4

Rate : $29/hr on W2 (without benefits)

POSITION SUMMARY

The Senior Process Technician drives the execution of Commercial, Clinical, and/or Development production according to Standard Operating Procedures and Production Schedule. The Senior Process Technician will work on interdisciplinary self-directed teams, to define and implement process improvements, participate in process troubleshooting.

JOB RESPONSIBILITIES

• Executes manufacturing operations on the production floor for buffer/media make-up tanks, glass washers, autoclaves, bioreactors, filtration equipment, inoculum preparation, chromatography skids and/or UF/DF skids with varying levels of automation.
• Executes the execution of SOPs for unit operations including but not limited to, CIPs, SIPs, Sanitization, etc.
• Implements the execution and issue resolution associated with process equipment commissioning, qualification and validation.
• Drives troubleshooting, technical support/analysis and resolution of equipment, automation, and process issues on the manufacturing floor.
• Drives for Right first time execution, the timely review of daily documentation and executes data entry; Monitor, Identify and/or Communicate process and compliance trends in real time.
• Supports the assigned audit lead for walkthroughs/GMP100s and observation improvements.
• View Role for controlled documentation; SOPs, Manufacturing Batch/Formulation Records, Forms, etc.
• Collaborates with the Subject Matter Expert for manufacturing operations in support of QTS investigations and CAPA implementations.
• Responsible for remaining current and reviews curriculum for training programs in support of manufacturing processes.
• Implements Lean Manufacturing, Sustainability, Operational Excellence initiatives; facilitate the drive towards continuous improvement in all manufacturing areas.
• Collaborates with cross-functional manufacturing assets in support of manufacturing campaigns.
• Collaborates in the escalation process through various levels of management when operations, personnel safety, equipment functionality, product supply and/or quality compliance are at risk.
• Ensures work requests are generated when issues arise with manufacturing equipment.
• Proficient in enterprise systems to support manufacturing operations including but not limited to, SAP, LIMS, AMPS, PDOCS and/or QTS.
• Operates production sustainability through the performance of inventory accuracy, reconciliation and/or task prioritization to maintain metric adherence.

MINIMUM QUALIFICATIONS

• High School diploma or greater required.
• 3-5 years of relevant experience

PREFERRED QUALIFICATIONS

• Experience in a GMP manufacturing environment is desired.
• Familiarity and experience with either purification processes or mammalian cell culture.
• Ability to interpret and prioritize workflow to maintain the production schedule.
• Effective verbal and written communication skills.

Pay: $28.00 - $29.00 per hour

Work Location: In person

Salary : $28 - $29