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Alcami

Pharmaceutical and biologics CDMO services

Technical Operations Specialist

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeClinton, TN, USANo salary listed

About the Job

Requirements

  • At least 5 years of experience in a pharmaceutical cGMP manufacturing setting is required.
  • At least 1 year of experience in technical writing, including deviations, standard operating procedures, and batch records, is required.
  • Demonstrated leadership and training experience is required.
  • Proficiency with Microsoft Office Suite, including Word, Excel, and PowerPoint, is preferred.
  • Ability to drive manufacturing operations and identify and improve inefficiencies.
  • Ability to work with people at all levels of the organization.
  • Ability to create and interpret graphs and charts.
  • Ability to solve practical problems and deal with concrete variables in situations where limited standardization exists.
  • Ability to interpret instructions furnished in written, oral, diagram, or schedule form.
  • Ability to write reports, business correspondence, and procedure manuals.
  • Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, and governmental regulations.
  • Ability to effectively present information and respond to questions from groups of managers and clients.
  • Basic knowledge of computers and Microsoft Office software products.
  • Ability to apply job skills, company policies, and standard operating procedures to complete a variety of tasks.
  • Ability to receive general instructions on routine work and detailed instructions on new projects or assignments.
  • Ability to meet the physical demands of the essential functions, including regularly handling objects, reaching, talking, hearing, and smelling; frequently sitting; occasionally standing, walking, and stooping, kneeling, crouching, or crawling; and lifting or moving up to 10 pounds regularly, 25 pounds frequently, and 50 pounds occasionally.
  • Required vision abilities include close, distance, and color vision, peripheral vision, depth perception, and the ability to adjust focus.
  • Ability to work with exposure to moving mechanical parts, vibration, fumes or airborne particles, toxic or caustic chemicals, and occasional wet or humid conditions, high or precarious places, or electrical-shock risk; wear appropriate personal protective equipment, including safety eyewear, hearing protection, respirators, lab coats, protective clothing, gloves, and, for elevated work, a body harness and lanyard; and potentially operate an industrial vehicle.

Responsibilities

  • Support commercial and clinical cGMP manufacturing operations by analyzing data to identify improvement areas and manufacturing trends.
  • Troubleshoot unexpected manufacturing events and production issues as a process subject matter expert, author investigations, and facilitate timely closure of investigations.
  • Ensure robust, reliable, and compliant product manufacturing.
  • Prepare, execute, and evaluate Continued Process Verification activities.
  • Monitor process performance and identify opportunities for improvement.
  • Provide ongoing technical support to manufacturing teams.
  • Partner with Technical Services, Operations, Quality, Engineering, and EHS teams to resolve documentation and manufacturing process issues resulting in corrective and preventive actions and process deviations.
  • Coordinate activities to align manufacturing functions.
  • Facilitate communication and issue resolution between departments.
  • Track and route documentation through required reviewers and approval channels, ensuring timely completion of document review and information accuracy.
  • Create and maintain standard work documents, including checklists, master batch records, and master production record templates.
  • Author change controls to support investigations, process changes, and equipment modifications.
  • Review and approve new batch records and review executed batch records.
  • Train manufacturing staff on operating procedures, batch records, and cGMP processes.

Desired Qualifications

  • A related bachelor's degree is preferred.
  • Proficiency with Microsoft Office Suite, including Word, Excel, and PowerPoint, is preferred.

About the Company

Alcami

Pharmaceutical and biologics CDMO services

Alcami is a contract development and manufacturing organization supporting pharmaceutical and biologics companies from early development through commercial production. Services span drug product manufacturing (sterile fill-finish and oral solid dose), analytical and microbiology lab testing, and cGMP storage with validation and environmental monitoring. What sets Alcami apart is its integrated, end-to-end capabilities across the development lifecycle. The goal is to help pharma and biotech partners deliver safe, high-quality therapies to patients.

Company size
51-200
Company stage
Not listed
Total funding
Not listed
Headquarters
Pepperell, MA
Founded
1984

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