MFG Associate, Downstream, Swing Shift, Fremont CA

Boehringer Ingelheim GmbH; Fremont (CA); On-site; USD 54,000 - 80,000; Full time

Benefits offered by this job

Discretionary bonus

Relocation assistance

Medical, dental and vision coverage

Job summary

Boehringer Ingelheim GmbH in Fremont, CA, is seeking a Manufacturing Associate for downstream operations on a swing shift (Sunday–Wednesday: 3:00 PM–1:30 AM PST; Wed 3:00 PM–11:30 AM). The role performs routine unit operations in a multi‑product facility, documents work per cGMP, and supports quality and safety programs.

The position requires a high school diploma and relevant GMP experience; an associate or bachelor’s degree is preferred.

Qualifications

• High school or equivalent required; cGMP experience preferred.
• Associates or Bachelor's degree in a related field preferred.
• One year or more in a GMP environment is desirable.

Responsibilities

• Operate routine downstream unit operations in a multi-product facility.
• Perform CIP/SIP, buffer prep, and sampling per SOPs and training.
• Document work in compliance with cGMP and cGDP standards.
• Support inventory, SOP updates, and safety practices.
• Train other technicians and contribute to quality investigations.

Education

High School Diploma

Associate's degree

Bachelor's degree

Job description

MFG Associate, Downstream, Swing Shift, Fremont CA

The base salary range for this position is $53,600 to $80,400. The position may be eligible for a role‑specific discretionary bonus, relocation assistance, and/or other compensation elements. We continuously review market data and may adjust salary ranges as needed in the future. Actual compensation will be based on job‑related factors such as skills, experience, qualifications, and other factors permitted by law. Benefits include medical, dental, and vision coverage, retirement savings opportunities, paid time off, paid holidays, disability and life insurance benefits, and other company‑sponsored benefits. For additional information regarding our benefits and Total Rewards offerings, please click here .

Description

Executes routine unit operations in Downstream manufacturing as assigned related to the manufacturing of bulk drug substance in a multi‑product facility. Performs duties under limited supervision and according to standard operating and manufacturing procedures. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work‑life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees

Swing shift Sunday‑Wednesday:

Sunday - Tuesday: 3:00 PM to 1:30 AM PST (overnight into the next day)Wednesday: 3:00 PM to 11:30 AM PST

Duties & Responsibilities

• Executes, with oversight of qualified staff, complex unit operations including but not limited to chromatography operations, tangential flow filtration, various filtration methods, and process monitoring.
• Executes independently with adequate training fundamental operations:
  • CIP/SIP of tanks, transfer lines, and process equipment.
  • Buffer preparation and transfer into tanks and disposables.
  • Performs In process testing for samples e.g. spectrophotometry, pH, conductivity, and maintenance of analytical equipment.
• This may include parts cleaning and weigh and dispense.
• Performs internal support duties including stocking consumables/materials, updating controlled SOP binders, appropriately discarding expired reagents, recognizing and reporting process and equipment anomalies.
• Documents work according to cGMP and cGDP.
• Adheres to established regulations and follows cGMP established by site.
• Reports abnormalities and deviations in a timely and accurate manner.
• Adheres to safety standards and identifies unsafe situations / habits and escalates appropriately.
• Maintains production areas according to predefined standards (5s).
• Maintains own training within compliance and trains other technicians and associates on operations upon completion of trainer qualification.
• Contributes to Quality activities as investigations and area walk‑throughs.

Requirements

• High school degree plus minimum one (1) year work experience in GMP regulated industry
• Associates/Bachelors degree from an accredited institution or biotechnology vocational training preferred.
• One (1) or more years of experience in cGMP regulated industry.
• Ability to concentrate on detail oriented work in a complex technical setup with a Quality and Right the first time mindset.
• Strong written and verbal communication skills.
• Ability to work with computer‑based systems and ideally experience with process control systems (e.g. Delta V) and manufacturing execution systems (MES).
• Ability to read and understand SOPs and work instructions and document work in a written format applying cGMP standards.
• Ability to work as part of a high performing team and collaborate effectively with staff.
• Basic knowledge of fundamental manufacturing concepts is preferred. Does not require extensive technical knowledge of manufacturing operations.
• Working in a highly regulated environment following all applicable BI and BI Fremont SOPs, OCPs and BGSs for cGMP, EHS and Compliance policies.
• Required to work according to given schedules in a 24/7 shift structure and flexibility to adapt working schedule upon prior given notice.