Full-Time

Senior Manager

Metrology

Posted on 9/10/2026

Deadline 9/10/27
Alcami

Alcami

51-200 employees

Pharmaceutical and biologics CDMO services

No salary listed

Morrisville, NC, USA

In Person

100% on-site, Monday through Friday, 8:00 a.m. to 5:00 p.m.

Bachelor's

Category
Manufacturing Quality & Test
Required Skills
Microsoft Office
Metrology

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Requirements
  • A related Bachelor's degree in Life Science, Engineering, or Electronics and 8+ years of relevant experience within the pharmaceutical industry.
  • At least 4+ years of experience in supervisory roles.
  • Knowledge of quality assurance reviews of metrology and validation documentation.
  • Training in current good manufacturing practices and understanding of current good manufacturing practice requirements.
  • Understanding of the pharmaceutical good manufacturing practice environment.
  • Ability to utilize Pro Cal.
  • Understanding of circuits, components, analytical equipment, and instrumentation for laboratory and manufacturing equipment.
  • Working knowledge of Microsoft Office applications, including Excel and Word.
  • Ability to supervise, train, and mentor employees.
  • Excellent mechanical skills.
  • Ability to train and mentor others.
  • Ability to listen and respond well to external customers, partners, and colleagues at all levels.
  • Ability to prioritize tasks according to business objectives and pursue several objectives simultaneously.
  • Ability to work independently with a high degree of self-motivation.
  • Ability to obtain support from different collaborators.
  • Ability to troubleshoot problems with enthusiasm and curiosity.
  • Ability to process information attentively and accurately.
  • Ability to wear appropriate personal protective equipment and access laboratory, manufacturing, or clinical areas for inspections or work discussions.
Responsibilities
  • Supervise the daily activities of the Metrology group performing calibrations, diagnostics, repair, maintenance, and equipment qualification of laboratory analytical instrumentation such as high-performance liquid chromatography and gas chromatography.
  • Develop production and resource plans that meet safety, quality, output, cost, and financial-savings goals.
  • Complete and review calibration documentation and the work of the Metrology team.
  • Support pharmaceutical metrology activities, including facility, utility, manufacturing equipment, and laboratory instrument metrology efforts.
  • Review, compose, and revise standard operating procedures and metrology master plans.
  • Conduct reviews of metrology documentation, including metrology plans, system and functional requirements, protocols, and summary reports.
  • Lead the Metrology department to optimize the qualification of equipment and systems.
  • Exercise judgment within defined procedures and practices to determine appropriate action.
  • Maintain documentation pertaining to qualification and metrology.
  • Develop procedures and protocols.
  • Lead investigations as needed.
  • Develop team metrics and ensure monthly goals are met.
  • Serve as an information resource for metrology personnel, contractors, and vendors.
  • Execute and oversee procedures and protocols.
  • Draft and approve department standard operating procedures and training modules.
  • Own the laboratory equipment requalification program and compliance with the program.
  • Act as a certified trainer for applicable training.
  • Ensure timely completion of and compliance with current good manufacturing practice and other relevant company training requirements.
  • Represent Alcami in client and regulatory audits regarding metrology-related questions.
  • Maintain the monitoring system for stability chambers and laboratory incubators.
  • Ensure adherence to personnel and equipment standard operating procedures and other regulatory requirements.
  • Monitor equipment operating practices and conditions to minimize downtime, lower maintenance costs, reduce project execution time, and reduce rework.
  • Develop and execute strategies to improve productivity.
  • Develop and execute work plans and schedules using production milestones and division or site performance standards and metrics.
  • Monitor progress against timelines.
  • Provide troubleshooting support as needed.
  • Monitor the quality of the group.
  • Communicate with clients and internal groups.
  • Attract, develop, and retain a high-performing team through selection, training and development, coaching and mentoring, and performance management.
  • Travel up to 10% as required.
Desired Qualifications
  • Familiarity with ISO 17025 and current industry calibration standards such as ASTM.

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

N/A

Total Funding

N/A

Headquarters

Pepperell, Massachusetts

Founded

1984

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Simplify Jobs

Simplify's Take

What believers are saying

  • Alcami acquired Tjoapack on May 5, 2026, expanding packaging reach into the Netherlands.
  • January 19, 2026 Durham facility purchase deepens biologics capacity for advanced services.
  • Revelio reported 1,038 employees in March 2026, showing hiring despite CEO turnover.

What critics are saying

  • February 6, 2026 FDA 483 at Charleston flagged sterile manufacturing controls and investigations.
  • Tjoapack integration strains management through 2026, with packaging line delivery only in 2027.
  • A sterile quality failure could shut Charleston operations and imperil Alcami's CDMO credibility.

What makes Alcami unique

  • Patrick Walsh keeps Alcami founder-level operator continuity after January 2025 CEO transition.
  • Durham RTP expansion adds fifth GMP fill-finish line and broad biologics analytical capacity.
  • Six-site U.S. GMP storage network gives Alcami integrated storage, testing, and manufacturing.

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Benefits

Remote Work Options

Company News

PR Newswire
Jan 13th, 2025
Alcami Announces Ceo Transition

Long time industry leader, Chairman of the Board Patrick Walsh replaces CEO Bill Humphries DURHAM, N.C., Jan. 13, 2025 /PRNewswire/ -- Alcami Corporation ("Alcami"), a leading contract development and manufacturing organization (CDMO), today announced the resignation of Bill Humphries. Alcami's Board Chair and former Chief Executive Officer Patrick Walsh will serve as Interim CEO, ensuring the continuation of smooth operations and a strong client-centric approach from a proven industry veteran

PR Newswire
Jul 23rd, 2024
Alcami Unveils New Conditions And Services At State-Of-The-Art Pharma Storage Facility In Garner

"Alcami's new facility is well positioned to fill previously unmet market demand," said Laurent Boer, President, Alcami Pharma Storage and Services. "The pipeline of complex medicines – exactly the type of ground-breaking products that life science companies in RTP work on – is only increasing. The biopharmaceutical materials and products in these drugs require very specific warehouse conditions that this new facility provides. But what truly sets us apart as a CDMO is our ability to offer a comprehensive pharma storage network paired with seamless access to our integrated laboratory and manufacturing services. From development to delivery, Alcami has the capabilities to care for and secure product within our own network, reducing risk and streamlining efficiency."After opening in January with controlled/ambient storage, the facility can now accept shipments for an extensive range of storage conditions, including stability chamber storage, refrigerated storage, freezer, ultra-low freezer, and cryogenic storage (LN2) as well as custom conditions. In addition, the site now offers a full suite of materials management and support services that facilitate the full product development, storage, and commercialization journey, including onsite aliquoting/sampling in grade C sampling booths, refrigerated transport, labeling, cycle counting/inventory management, custom kitting, and reference standards management.The new central North Carolina facility adjacent to the Research Triangle Park expands Alcami's high-quality, secure GMP storage network to six U.S

Contract Pharma
Dec 15th, 2021
alcami acquires Masy Systems Inc.

Alcami Corp., a pharmaceutical and biotech contract development and manufacturing organization ( CDMO ), has completed the acquisition of Masy Systems Inc., a provider of cGMP biostorage and pharma support services.

PR Newswire
Dec 15th, 2021
AAIPharma Services Corp. acquired Masy Systems Inc. on Dec 15th 21'.

Alcami Corporation, a leading pharmaceutical and biotech contract development and manufacturing organization (CDMO), announced today it has completed the acquisition of Masy Systems Inc. ("Masy" or "Masy BioServices"), a preferred provider of cGMP Biostorage and pharma support services.

Daily Times Chronicle
Dec 1st, 2021
Masy Systems Inc. launches SenseAnywhere modules

Masy BioServices announces the launch of innovative SenseAnywhere modules.