Life Sciences Production Technician
Life Science Production Technician - 1 year renewable contractLocation:
100% onsite - Gaithersburg, MDShift:
1st, 6:
30am - 3:
30pm, Mon-FriRespirator hood will need to be worn on certain processing days (30% of the time)Will be working with Antibiotic Antigen Manufacturing TechnologyGreat entry level opportunityMust haves:
Associates or Bachelor's in Life Sciences, Engineering, Biology, Biochemistry or related fieldEntry to mid level experience (1-2 years of experience of Biotech experience in leu of degree)Description of PositionAs a pilot production associate in the Clinical production team within Biopharmaceutical Development, you'll build broad knowledge of bioprocessing in a cGMP environment to launch your career in the biopharmaceutical industry.
In this role you will take an adaptable, science driven approach to everything you do.
You will become an integral part of process development, accelerating product candidates into the clinic and gaining knowledge and experience in cell culture, purification and critical support activities.
Under the supervision of highly trained personnel, you will gain the process knowledge and skillsets to perform large scale clinical development activities through hands-on training.
You will join a collaborative and driven team in a world class biopharmaceutical company that is driving disruptive innovation in the industry.
Principal Duties Serves as a trainer for the bio-pharmaceutical manufacturing equipment such as:
incubators, stainless steel and disposable single-use bioreactors, depth filtration skids, LN2 dewars, chromatography skids, single-use mixers, centrifuges, cleaning/sanitization of equipment, washers, autoclaves, environmental monitoring cleaning verification sampling, tanks and in-process testing instruments.
Monitors critical process parameters, troubleshoots during processing and recommends potential solutions to management.
Serves as the Subject Matter Expert in unit operation to improve quality, ensure safety and process efficiency/accuracy Contributes to the development of new concepts, techniques, standard operation creation/revise and standards Reviews executed Production Records for accuracy and completion of process steps within a GMP/GMP manner Ability to utilize MS Office tools and AZ enterprise systemAdditional Principal Duties based on Core GroupPurification Technical Principal Duties Introductory knowledge of Column Chromatography process operations, column packing TFF (Tangential Filtration Flow) and basic analytical testing (eg Protein concentration, osmolarity, pH etc.
) Introductory knowledge of antibody conjugation processes in a single use isolatorCell Culture Technical Principal Duties Prepare stainless steel and disposable bioreactors and tanks to include Pressure Test, CIP, SIP, and Centrifuge Harvest Perform aseptic technique and cell banks operations Prepare and charge the LN2 Dewar's for vial shipmentSupport Services Technical Principal Duties Preparation and filtration of production scale buffer and media solutions.
Operate area specific production equipment such as glass washers, autoclaves, fixed and portable stainless steel tanks, etc.
Weighs and checks raw materials, assembles and cleans process equipment, monitors processesAll Stream Proficient in cell culture operations such as biosafety cabinet operation, bioreactor operations (eg tabletop bioreactor and single use bioreactors) and centrifuge harvest operations Proficient raw material weight-out and media/buffer preparation Proficient in the operation of all area specific production equipment such as column chromatography operations, tangential flow filtration, formulation and column packing Proficient in basic analytical testing (eg protein concentration, osmolarity, pH and etc.
)Desired Skills:
Dynamic individual with the ability to communicate and engage others.
Independent and self-starting.
Ability to work with minimal supervision.
Demonstrate a high level of drive and initiative.
Logic and decision-making abilities, critical thinking and troubleshooting skills.
Demonstrate leadership, organization and time management skills.
Demonstrate flexibility and willingness to change ways of working/identify opportunities to improve processes within cGMP clinical manufacturing environment.
Proficient in antibody conjugation process and manual operation in a glove box isolator unit.
#LI-JL1SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
100% onsite - Gaithersburg, MDShift:
1st, 6:
30am - 3:
30pm, Mon-FriRespirator hood will need to be worn on certain processing days (30% of the time)Will be working with Antibiotic Antigen Manufacturing TechnologyGreat entry level opportunityMust haves:
Associates or Bachelor's in Life Sciences, Engineering, Biology, Biochemistry or related fieldEntry to mid level experience (1-2 years of experience of Biotech experience in leu of degree)Description of PositionAs a pilot production associate in the Clinical production team within Biopharmaceutical Development, you'll build broad knowledge of bioprocessing in a cGMP environment to launch your career in the biopharmaceutical industry.
In this role you will take an adaptable, science driven approach to everything you do.
You will become an integral part of process development, accelerating product candidates into the clinic and gaining knowledge and experience in cell culture, purification and critical support activities.
Under the supervision of highly trained personnel, you will gain the process knowledge and skillsets to perform large scale clinical development activities through hands-on training.
You will join a collaborative and driven team in a world class biopharmaceutical company that is driving disruptive innovation in the industry.
Principal Duties Serves as a trainer for the bio-pharmaceutical manufacturing equipment such as:
incubators, stainless steel and disposable single-use bioreactors, depth filtration skids, LN2 dewars, chromatography skids, single-use mixers, centrifuges, cleaning/sanitization of equipment, washers, autoclaves, environmental monitoring cleaning verification sampling, tanks and in-process testing instruments.
Monitors critical process parameters, troubleshoots during processing and recommends potential solutions to management.
Serves as the Subject Matter Expert in unit operation to improve quality, ensure safety and process efficiency/accuracy Contributes to the development of new concepts, techniques, standard operation creation/revise and standards Reviews executed Production Records for accuracy and completion of process steps within a GMP/GMP manner Ability to utilize MS Office tools and AZ enterprise systemAdditional Principal Duties based on Core GroupPurification Technical Principal Duties Introductory knowledge of Column Chromatography process operations, column packing TFF (Tangential Filtration Flow) and basic analytical testing (eg Protein concentration, osmolarity, pH etc.
) Introductory knowledge of antibody conjugation processes in a single use isolatorCell Culture Technical Principal Duties Prepare stainless steel and disposable bioreactors and tanks to include Pressure Test, CIP, SIP, and Centrifuge Harvest Perform aseptic technique and cell banks operations Prepare and charge the LN2 Dewar's for vial shipmentSupport Services Technical Principal Duties Preparation and filtration of production scale buffer and media solutions.
Operate area specific production equipment such as glass washers, autoclaves, fixed and portable stainless steel tanks, etc.
Weighs and checks raw materials, assembles and cleans process equipment, monitors processesAll Stream Proficient in cell culture operations such as biosafety cabinet operation, bioreactor operations (eg tabletop bioreactor and single use bioreactors) and centrifuge harvest operations Proficient raw material weight-out and media/buffer preparation Proficient in the operation of all area specific production equipment such as column chromatography operations, tangential flow filtration, formulation and column packing Proficient in basic analytical testing (eg protein concentration, osmolarity, pH and etc.
)Desired Skills:
Dynamic individual with the ability to communicate and engage others.
Independent and self-starting.
Ability to work with minimal supervision.
Demonstrate a high level of drive and initiative.
Logic and decision-making abilities, critical thinking and troubleshooting skills.
Demonstrate leadership, organization and time management skills.
Demonstrate flexibility and willingness to change ways of working/identify opportunities to improve processes within cGMP clinical manufacturing environment.
Proficient in antibody conjugation process and manual operation in a glove box isolator unit.
#LI-JL1SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
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