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Lancesoft is seeking a Bioprocess Manufacturing Technician to operate in a highly automated, cGMP environment across production areas, including upstream/downstream processes. The role involves following SOPs and manufacturing documentation while maintaining accurate records and safety compliance.
The position is a contract role with potential conversion to permanent employment. Training includes shift rotations and 24x7 facility coverage, with competitive hourly pay and facility onboarding.
As a Bioprocess Manufacturing Technician, you will be responsible for producing medicine in a highly automated and controlled environment. Each product has a specific recipe;you will follow this recipe, along with the standard operating procedures, to operate the production equipment across various areas, including raw material dispensing/aliquoting, cell culture and purification. You will maintain records and follow all the steps necessary to comply with regulatory requirements within a current Good Manufacturing Practices (cGMP) environment. This is a contract role with the possibility of conversion to a permanent employee position. We have both Stainless Steel and Single-Use Manufacturing facilities that are supported by Production Services. There are 3 main production areas within manufacturing: Production Services - Responsible for weighing and aliquoting of raw materials and small scale solution prep. Also responsible for washing, autoclaving, and preparation of small equipment parts and assemblies. Responsible for environmental monitoring of the facility. Upstream Manufacturing - Responsible for cell growth from inoculation in spinner flasks through large scale bioreactors and the harvesting of cell culture via centrifugation and depth filtration. Downstream Manufacturing - Responsible for the purification of cellular harvest utilizing chromatography and reformulation techniques, as well as preparation of product for shipping to final fill/finish sites. As a new member of the team, you ll typically be assigned to one of the three production areas. This will allow you to build capabilities and work on increasingly complex technical assignments, with the potential to rotate into future production areas as you gain experience.
Safety is paramount to both our employees and our patients, and is therefore at the core of all job responsibilities. This includes complying with all safety requirements, cGMP, Standard Operating Procedures (SOP) and manufacturing documentation. You must immediately report any and all safety and environmental incidents, including injuries, illness, near miss & safety suggestions.
You re a quick learner and can receive, digest and interpret instructions with ease You re technically and mechanically inclined and can learn new systems and technology quickly You find joy in the details and pride yourself in accuracy You can work independently but as part of a larger team You can demonstrate the ability to independently document and record information You showcase good judgment and ability to recognize non-routine problems/deviations and elevate partner on potential solutions You demonstrate increasing technical competency through training and operational procedures of at least one manufacturing department You manage your time and communicate effectively with your team members.
We have a variety of 12- and 10-hour shifts to support our 24x7 facility operations. Staff working over 8 hours in a day will be paid overtime in accordance with local and state laws. In addition, staff working swing or night shifts will be paid a shift differential. While we are occasionally able to accommodate shift requests, candidates with open availability will be given priority consideration as we are not able to guarantee shift placement. Candidates must be able to work any of the following manufacturing shifts: 10 hr Day Shift, 6: 00 am 4: 30 pm Sunday - Wednesday or Wednesday - Saturday 10 hr Mid Shift, 10: 00am-08: 30PM Sunday - Wednesday or Wednesday - Saturday 10 hr Swing Shift, 12: 30 pm -11: 00 pm Sunday - Wednesday or Wednesday - Saturday 10 hr Swing Shift, 1: 30 pm -00: 00 am Sunday - Wednesday or Wednesday - Saturday
Onboarding will consist of a 3-4 week schedule of Monday thru Friday 8am - 5pm followed by on the job training on the respective shift schedule.
Proficiency in the English language- reading, writing, and communication. Must be computer literate due to the extensive automation used in our facility, experience with Microsoft and Google platforms. Must be able to work all shifts, required overtime as needed, and stand for extended periods of time. Our facility is expansive - you may climb multiple flights of stairs daily Lifting up to 25 lbs is required. The cleanroom environment requires gowning in the form of cleanroom scrubs, bunny suits, gloves, hair covers, safety glasses, and steel toe boots be worn. No makeup or jewelry can be worn when working in the clean room environment. Personal electronic devices (e.G. Cell phones) are not permitted in cleanrooms without formal approval due to health authority regulation. You may work with hazardous materials and chemicals Must be able to successfully pass all job-related tests and certifications required for working in a cGMP, quality environment including but not limited to: inspections and GMP requirements to perform essential functions of the job.
High school diploma or equivalent Preferred - Degree in Life Sciences/Engineering, Associate s or Biotech certificate from approved program
To learn more about the manufacturing process, please watch this video: strong style="box-sizing: inherit;margin: 0px;padding: 0px;"]https://www.Youtube.Com/watch? V=sxvJatvqBVE
Please note: We currently do not sponsor work visas for this position or offer relocation assistance.
The expected salary range for this position based on the primary location of California is ***/hour. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.