Sr. Manufacturing Technician

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

Benefits offered by this job

Annual bonus

401k matching

Gym subsidy

Paid time off

Tuition assistance

Job summary

Partner Therapeutics, Inc. is seeking Senior Manufacturing Technicians to support cGMP operations, cleaning and sterilization of equipment, and upstream or downstream processes.

The role involves operating fermenters, chromatography systems, autoclaves, and media preparation under SOPs, with emphasis on compliance, teamwork, and quality. A high school diploma or GED is required, with preferred biopharma experience and potential hybrid/remote work options.

Qualifications

• Requires High School Diploma or GED.
• Experience in a cGMP manufacturing environment preferred.

Responsibilities

• Operate fermentation systems and chromatography equipment per SOPs.
• Perform clean-in-place and steam-in-place operations.
• Prepare media and buffers, weigh and mix ingredients.
• Carry out routine equipment maintenance and keep area tidy.
• Follow SOPs, GMP, safety and regulatory guidelines.

Skills

PPE compliance

Safety awareness

Teamwork

Problem solving

Verbal & written communication

MS Office

English proficiency

Education

High School Diploma or GED

Associate/Bachelor degree in science/engineering

Tools

MS Word & Excel

Job description

POSITION SUMMARY

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 requiredtimeframes.


• 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,exhibitsa consistently constructive attitude, and is adaptable and at ease with handling unexpectedchanges andchallenges.


• Solid English languagecommunicationskills, both oral and written, arerequiredfor this highly collaborative role. Willingness and ability to clearly express opinions and ask questions.Comfortable activelyparticipatingin cross-functional meetings.


• Proficiencywith 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

• 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 computer 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.