Operations Specialist

We seek an Operations Specialist to support the Pilot Bioproduction Facility (PBF) at the Walter Reed Army Institute of Research (WRAIR) in Silver Spring Maryland. The Operations Specialist will support manufacturing in the following areas Upstream Downtime Purification and Fill Finish. PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next-generation development for cutting-edge companies and government agencies. The professionals at PBF are engaging in trailblazing endeavors every day. Most exciting the end products vary so every year brings multiple opportunities for professional enrichment in original projects.

CAMRIS International LLC is a dynamic medical research and development firm that achieves innovative solutions to health and development challenges through high-quality cost-effective programs and research management services. We combine our proven systems with todays most effective evidence-based best practices. Our core practice areas include vaccine research development and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS programs.

Our employees enjoy a collegial environment where individual contributions matter at all levels. At CAMRIS you will notably improve the lives of people at home and abroad.

Upstream: Prepare cell culture for virus inoculation and prepare viral seeds.

• Provide input on cell culture bioproduction and purification of mammalian cell-based products.
• Experience and knowledge of cGMP specifically bioproduction of viral vaccines.
• Execute and participate in cGMP viral growth virus vaccine purification for cGMP vaccine bioproduction.
• Aseptic gowning aseptic processing aseptic final filtration and working in a cleanroom environment.
• Cell culture experience (adherent cells a plus) washing and counting cells repeated trypsin manipulations.
• Maintain virus vaccine bioproduction inventory order equipment and reagents.

Downstream: The downstream part of a bioprocess refers to the part where the cell mass from the upstream are processed to meet purity and quality requirements.

• Execute cell expansion of seeds and viral seeds as required.
• Manage and maintain manufacturing-owned controlled temperature units (CTUs) and incubators per site policies and procedures.
• Perform bioreactor setup operation maintenance and cleaning per site policies and procedures.
• Prepare harvest equipment per SOP and batch record instructions per site policies and procedures.
• Execute cell lysis through chemical or physical (e.g. microfluidizer) cell disruption.
• Perform recovery mid-stream unit operations including but not limited to depth filtration centrifugation and tangential flow filtration as required and per site policies and procedures.
• Pour resin pack columns verify HETP and Asymmetry and equilibrate columns.
• Develop purification batch records and AKTA UNICORN methods as required.
• Analyze UNICORN and other downstream result files attach per GDP to records summarize data and incorporate analysis into run reports as required.
• Sanitize empty and store columns per site policies and procedures.

Purification: Separation of contaminants closely imitating the product in physical and chemical properties.

• Prepare buffers pour columns with specific resins lyses cells to homogeneous suspensions.
• Perform extractions of cells and cell products.
• Use column chromatography centrifugation and other techniques to purify vaccine materials.
• Make recommendations for the purification of desired products based on research data received from research personnel.
• Responsible for all types of purification and downstream processing and the use of various equipment to meet these goals.
• Perform various analytical procedures to characterize and quantitate the product at all steps in the purification process.

Fill Finish: Filling Formulation and Lyophilization of desired products.

• Perform scheduling of filling/lyophilization of desired products.
• Perform bulk thaw dilution and formulation operations.
• Set up equipment/machines aseptically for proper operation including installing and disassembling equipment and parts required for filling and formulation operations.
• Perform all documentation and clerical functions to provide the proper accountability and traceability of components and finished product.
• Operate cleanroom equipment aseptically and efficiently (lyophilizer manual and automated filler equipment vial washer part washer autoclave labeler and dehydrogenation oven).
• Perform full-scale lyophilization of vaccine lots including monitoring cycle parameters while in process.
• Perform labeling of final product vials.
• Operation and non-contract maintenance of the filling machines freeze-dryer and sterilization equipment; preparation of all glassware reagents and materials that are used for a filling operation.

General Duties:

• Adheres to current Good Manufacturing Procedures (cGMP) guidelines and FDA regulations as they apply to all levels of work.
• Assist in writing Standard Operating Procedures and production batch production records.
• Adept at problem-solving. Specifically in identifying problems developing solutions executing remedies and elevating problems to management if necessary.
• Follow basic safety/EHS requirements SOPs cGMP work rules and other company policies.
• Maintains a safe workplace ensuring that he/she is aware of and observes appropriate safety and occupational health rules and regulations. Employee is required to attend safety training related to his/her position and report any infractions of safety procedures to the facility Safety Officer.
• Performs light duties and other related duties as required and assigned.
• Must have proficiency with various types of office software: Outlook Word Excel. MS Project; LIMS experience and experience with equipment monitoring systems are a plus.
• Must have the ability to follow directions written policies and procedures for work responsibilities.
• Licensed vaccinations might be required to work with certain viral agents.
• Must have good people and communication skills (written and verbal).
• Performs other duties as required.

• A bachelors degree in a science field (preferably chemistry biochemistry microbiology or engineering) and four years of industry experience performing cGMP production downstream purification fill finish and upstream in a clean room environment.
• Professional knowledge and experience requirements related to viral product safety for product release and downstream purification (chromatography) a plus.
• Experience with aseptic gowning aseptic processing aseptic final filtration and working in a cleanroom environment.
• Experience with bioproduction equipment: centrifuges tangential flow filters spectrophotometer biosafety cabinets sonicator autoclave roller bottles a plus.
• cGMP experience for large-scale viral production of biological products a plus.
• Working knowledge of disposable manufacturing methodologies such as the use of sterile bags with tubing and tubing welders is a definite plus.
• Hepatitis B immunity is required; vaccination will be provided if needed.
• Must be able to work independently following a brief period of specific technical training.
• Must have familiarity with related fields such as general microbiology physical chemistry and biochemistry.
• Must have some knowledge of the operation of automated/manual filling machines Restricted Access Barrier System (RABS) and labeling machines.
• Experience in filling parenteral products under GMP conditions.
• Must have eligibility to work in the United States and have lived in the United States for three of the past five years if a non-US citizen.

Physical Requirements:

The physical requirements described here are representative of those that must be met by a candidate to perform the essential functions of this job. Reasonable accommodations may be provided to enable individuals with disabilities to perform essential job functions.

• Occasionally required to perform sedentary work that primarily involves sitting/standing.
• Constantly required to perform light work that includes moving objects up to 20 pounds.
• Occasionally required to perform medium work that includes moving objects up to 50 pounds heavy work that includes moving objects up to 100 pounds and very heavy work that includes moving objects over 100 pounds.
• Occasionally required to push or pull less than 25 pounds push or pull 25 45 pounds and push or pull more than 45 pounds.
• Occasionally required to reach above shoulder level use both hands and stand or walk for more than 25 minutes.
• Occasionally required to bend reach or twist repeatedly kneel squat or stoop and crawl or climb.
• Constantly required to have clear vision (near and/or far) depth perception peripheral vision and/or visual acuity.
• Occasionally required to ascend or descend ladders stairs scaffolding ramps poles and the like and move self in different positions to accomplish tasks in various environments including tight and confined spaces.
• Constantly required to move about to accomplish tasks or move from one worksite to another.
• Occasionally required to communicate with others to exchange information.
• Occasionally required to operate machinery and/or power tools and operate motor vehicles or heavy equipment.
• Constantly required to assess the accuracy neatness and thoroughness of the work assigned.
• Occasionally required to work in outdoor elements such as precipitation and wind noisy environments and hazardous conditions.
• Occasionally required to work in poor ventilation small and/or enclosed spaces and no adverse environmental conditions expected.
• Constantly required to wear PPE including but not limited to gloves face shields/goggles safety glasses and safety shoes.
• Occasionally required to usea lab coat and ear plugs/muffs.
• Constantly required to wear a clean room uniform.
• Occasionally required to use a disposable dust/surgical mask and respirators such as a disposable respirator mask (N-95) half-face/full-face style PAPR SCUBA.
• Constantly required to come in contact with chemicals such as aerosols biological inhalants plastics inorganic dust and powders etc.

Please submit your resume online at . CAMRIS is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin age protected veteran status disability status or any other characteristic protected by any applicable federal state or local law.

CAMRIS offers a comprehensive benefits package including medical dental and vision insurance for individuals and families FSAs HSA life and AD&D insurance short- and long-term disability legal services voluntary hospital indemnity critical illness and accident insurances EAP pet insurance 401(k) with employer match and Roth option tuition and professional reimbursement public transportation support in the DMV area a referral bonus program vacation with tenure-based increases PTO 11 paid holidays paid bonding leave and paid supplemental short-term disability.

Employment is contingent upon successful completion of a Public Trust-level background check a requirement for this position under an active federal contract. The background check process may include but is not limited to the following: (1) contacting your professional references; (2) verification of previous employment education and credentials; (3) a criminal background check; (4) use/abuse of federally-controlled substances; and (5) a department of motor vehicle check. Candidates must be prepared to fully-complete any required background check questionnaire during initial onboarding.