Sr. Manufacturing Technician (Onsite)

Partner Therapeutics, Inc.; Lynnwood (WA); Hybrid; USD 60,000 - 72,000; Full time

Benefits offered by this job

Hybrid/Remote workplace program

Annual bonuses

401k matching

Wellness program

Paid time off

Gym subsidy

Tuition assistance

Free parking

Orca pass

Job summary

Partner Therapeutics, Inc. in Lynnwood, WA is seeking Senior Manufacturing Technicians to support cGMP operations, upstream (fermenters and filtration) and downstream (HPLC and low-pressure chromatography) activities.

You will perform a variety of GMP tasks, operate production equipment per SOPs, prepare media and buffers, conduct CIP/SIP, test filters, maintain clean areas, comply with safety standards, and complete required training on time.

Qualifications

• High School Diploma or GED required.
• 2+ years of relevant work experience or certification/degree in biopharmaceutical manufacturing.
• Associate or BA/BS in science/engineering preferred.
• GMP/cGMP manufacturing environment experience is a plus.

Responsibilities

• Operate process equipment (fermenters, chromatography systems) per SOPs.
• Operate autoclaves, media and buffer prep equipment per SOPs.
• Perform CIP/SIP to prepare equipment for manufacturing.
• Prepare media and buffers (weighing, measuring, mixing, filtering).
• Test filter integrity and perform regular equipment maintenance.
• Maintain tidy, compliant work area and follow safety policies.
• Complete mandatory Quality and Compliance training on schedule.
• When not manufacturing Leukine, revise controlled documents and maintain training.

Skills

Respirator use

PPE compliance

Problem solving

Teamwork

English communication

MS Office

Education

High School Diploma or GED

Associate degree in science/engineering (preferred)

BA/BS in science/engineering (preferred)

Tools

MS Office

Job description

Senior Manufacturing Technicians are involved in cleaning and sterilization of process equipment and supporting cGMP operations. Upstream staff focuses on supporting fermenters and filtration equipment, Downstream staff focuses on supporting HPLC and low-pressure Chromatography equipment.

PRIMARY RESPONSIBILITIES

• This position is responsible for performing a variety of manufacturing tasks under general guidance and in accordance with current GMPs. Responsibilities include:
• Operates process equipment such as fermenters and chromatography systems in accordance with established Standard Operation Procedures (“SOP”s)
• Operates support equipment such as autoclaves, media and buffer preparation equipment in accordance with established SOPs
• Performs clean-in-place and steam-in-place operations to prepare equipment for manufacturing operations in accordance with established SOPs
• Media/buffer compounding (weighing, measuring, mixing, filtering)
• Filter wetting and integrity testing
• Stocking of materials and equipment
• Performing basic maintenance of equipment
• Maintains tidiness of area
• Adheres to all applicable regulations and requirements including compliance with internal SOPs, GMP, Health and Safety, WISHA/OSHA, regulatory compliance, company policies, and employment-related laws and statutes.
• Successfully completes all mandatory Quality and Compliance training within required timeframes.
• When the facility is not actively manufacturing Leukine, the technician will be responsible for the following:
• Revision of controlled documents
• Maintaining training and acquiring new skills
• Performing routine maintenance on Manufacturing equipment and systems

KNOWLEDGE, SKILLS, ABILITIES

Required:

• Ability and willingness to wear a respirator and other PPE for multiple consecutive hours while meeting compliance and safety guideline to complete certain tasks.
• Ability and willingness to work with strong acids, bases, and other solvents required for the job (PPE utilized).
• Meets training and qualification requirements, including proficiency assessments.
• Ability and willingness to follow directions from others (i.e., peers, lead, supervisor).
• Possesses effective problem solving and teamwork skills.
• Recognizes severity of issues and escalates to a Supervisor or higher level co-worker as appropriate.
• Utilizes manufacturing knowledge to improve operations and affect positive change.
• Excellent soft skills including a bias towards action, the ability and willingness to give and receive constructive feedback, is comfortable working within a diverse team and across multiple functions, exhibits a consistently constructive attitude, and is adaptable and at ease with handling unexpected changes and challenges.
• Solid English language communication skills, both oral and written, are required for this highly collaborative role. Willingness and ability to clearly express opinions and ask questions. Comfortable actively participating in cross-functional meetings.
• Proficiency with MS Office products including Word and Excel necessary; ability and willingness to quickly adopt other job-specific applications will be necessary.

Preferred:

• Experience in Fermentation/Upstream (microbial fermentations, filtration equipment) and/or Downstream experience (HPLC and low-pressure Chromatography)

EXPERIENCE & EDUCATION

Required:

• High School Diploma or GED
• 2 + years of relevant work experience. Some work experience can be substituted/augmented with achievement of a relevant certification in biopharmaceutical manufacturing program, an associate or bachelor's degree from an accredited institution.

Preferred:

• Associate degree, BA or BS in a science-related field or Engineering Field.
• Experience in a cGMP manufacturing environment or other comparable experience (i.e., other regulated industry)

SPECIAL WORKING CONDITIONS

• Special Physical Requirements (lifting, pushing/pulling, climbing, fine motor skills, driving, etc.):
• Prolonged walking and/or standing.
• Lifting 15 kilograms (30 pounds) successfully without assistance.
• PPE required including prolonged use of a fitted respirator.
• Ability to meet PTx gowning requirements to work in a Grade C/D cleanroom (ISO class 7/8).
• Ability to work with strong acids, bases, and other solvents required for the job (PPE utilized).
• Some seated work in front of video monitors

PTx is committed to the principles of pay equity and providing competitive compensation for all of our Partners. The current pay range for this position is $60,000 - $72,000: Offers are made within the base pay range applicable at the time. Your salary will vary depending on several factors including your qualifications and experience.

In addition to medical, dental, vision, FSA/DCA, HRA, disability, and life insurance coverage, all full-time, regular Partners enjoy a casual, and Hybrid or Remote workplace program for many roles. We offer a terrific compensation/benefits/perks package which includes an annual cash bonuses, 401k matching, free parking, Seattle-area ORCA pass, tuition assistance, plus rewards for achievement and contribution. To support a healthy work-life balance we also provide a gym subsidy, wellness participation programs, and a generous vacation, sick, and holiday paid time off program in addition to a paid shutdown between the Christmas and New Year’s holidays.

Partner Therapeutics is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, sex, age, national origin, veteran status, marital status, sexual orientation, gender identity, disability or any other category prohibited by local, state, or federal law. This policy applies to all aspects of employment, including recruitment, placement, promotion, transfer, demotion, compensation, benefits, social and recreational activities, and termination.