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Manager Biotech Quality Control Jobs in Springfield, MA

Rotating Machinery Svcs Inc

Quality Manager

Chicopee, MA · On-site

$110K - $120K/yr

THE ROLE We are seeking a Quality Manager to join our Quality Assurance/Control team. The Quality Manager is responsible for monitoring, evaluating, and improving RMS's Quality Management programs ...

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Quality Assurance Manager

Holyoke, MA · On-site

Oversee the facility's QA/QC department and ensure all employees understand and follow all standard ... Partner with management to lead quality initiatives that develop and maintain a high performing ...

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Quality Assurance Manager

Holyoke, MA · On-site

The Role The Quality Assurance Manager is responsible for managing and enforcing all quality ... Oversee the facility's QA/QC department and ensure all employees understand and follow all standard ...

Cadrex Agawam

Supervisor - Quality

Agawam, MA

$96K - $115K/yr

Oversee the quality control operations, ensuring adherence to quality standards, procedures, and regulatory requirements * Manage a team of quality inspectors, providing leadership, guidance, and ...

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All JobsManager Biotech Quality Control JobsManager Biotech Quality Control Jobs in Springfield, MA

Manager Biotech Quality Control information

See Springfield, MA salary details

$30.4K

$81K

$129K

How much do manager biotech quality control jobs pay per year?

As of Jun 29, 2026, the average yearly pay for manager biotech quality control in Springfield, MA is $81,039.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,300.00 and $99,600.00 per year, depending on experience, location, and employer.

What is the difference between Manager Biotech Quality Control vs Quality Control Specialist?

AspectManager Biotech Quality ControlQuality Control Specialist
CredentialsBachelor's/Master's in Life Sciences, Quality Certifications (e.g., CQE)Bachelor's in Life Sciences or related field, Quality Certifications preferred
Work EnvironmentOversees QC teams, manages testing processes, and ensures compliancePerforms testing, data analysis, and reports results
Employer & Industry UsageBiotech companies, pharmaceutical firms, contract labsBiotech, pharma, and manufacturing sectors

The Manager Biotech Quality Control typically oversees testing teams and ensures compliance with quality standards, while the Quality Control Specialist focuses on executing tests and analyzing data. Both roles require relevant scientific credentials, but the manager has additional responsibilities in team leadership and process management.

What does a Manager Biotech Quality Control do?

A Manager Biotech Quality Control oversees the quality assurance processes within a biotechnology company, ensuring that products meet regulatory standards and internal specifications. They manage teams responsible for testing raw materials, in-process samples, and finished products, and analyze data to identify trends or issues. This role also involves setting quality control policies, training staff, and liaising with regulatory bodies to maintain compliance. Managers in this field play a crucial role in product safety and efficacy, directly impacting the success of biotech products in the market.

What are the most common challenges faced by a Manager in Biotech Quality Control, and how are they typically addressed?

Managers in Biotech Quality Control often face challenges such as ensuring regulatory compliance, maintaining rigorous documentation, and managing a team with diverse expertise. Keeping up-to-date with changing industry standards and regulatory requirements is crucial, as is fostering a culture of continuous improvement and clear communication. These challenges are typically addressed through ongoing staff training, implementing robust quality management systems, and close collaboration with other departments like R&D and manufacturing to ensure that quality standards are consistently met.

What are the key skills and qualifications needed to thrive as a Manager Biotech Quality Control, and why are they important?

To thrive as a Manager Biotech Quality Control, you need a strong background in biology or chemistry, extensive knowledge of quality assurance regulations, and typically a bachelor’s or master’s degree in a life science field. Familiarity with laboratory information management systems (LIMS), GMP (Good Manufacturing Practices), and certifications such as ASQ or Six Sigma are highly valued. Leadership, attention to detail, and strong problem-solving and communication skills help you guide teams and ensure compliance. These skills and qualities are critical for maintaining product quality, regulatory adherence, and the overall success of biotech manufacturing operations.
What job categories do people searching Manager Biotech Quality Control jobs in Springfield, MA look for? The top searched job categories for Manager Biotech Quality Control jobs in Springfield, MA are:
What cities near Springfield, MA are hiring for Manager Biotech Quality Control jobs? Cities near Springfield, MA with the most Manager Biotech Quality Control job openings:
Manager Biotech Quality Control jobs near you

Quality Manager

Rotating Machinery Svcs Inc

Chicopee, MA • On-site

$110K - $120K/yr

Full-time

Posted yesterday

Job description

Rotating Machinery Services


Quality Manager

Shop Environment

Chicopee, MA – Exempt – Full Time


ABOUT ROTATING MACHINERY SERVICES

Rotating Machinery Services (RMS) was established in 1998 with the vision to reinvent the concept of an aftermarket turbomachinery business. The goal was to provide turbomachinery operators with unparalleled service built on established relationships, solid engineering, and technical expertise backed by responsiveness, competitive pricing, and lead times.


RMS’s commitment to quality penetrates every aspect of the organization and is the guiding force for all decision-making. With an equal blend of cutting-edge technology, engineering expertise, and skilled craftsmanship, RMS consistently delivers the best possible results for customers. RMS is a nimble organization with a collaborative culture of individuals who come to work every day with a desire to improve upon their craft and further the rotating machinery industry.


THE ROLE

We are seeking a Quality Manager to join our Quality Assurance/Control team.


The Quality Manager is responsible for monitoring, evaluating, and improving RMS’s Quality Management programs and processes. This position provides Quality leadership to the site processes to promote and continually improve the quality culture. The Quality Manager shall promote strong employee and customer relationships pertaining to quality compliance.


SKILLS REQUIRED

ORGANIZATIONAL

LEADERSHIP AND ORGANIZATION

  • Strong leadership presence with the ability to influence and hold colleagues accountable at all levels—from the shop floor to senior management.
  • Detail-oriented and process-driven, with the discipline to maintain documentation standards under production schedule pressure.

INTERPERSONAL

EXPERIENCE REQUIRED

  • Skilled communicator—able to present quality data clearly, write concise technical reports, and represent RMS professionally with customers and auditors.
  • Collaborative, solutions-focused mindset; comfortable working in a fast-paced, custom-work environment.
  • Willingness to work on the floor alongside the QC team rather than managing from a distance.

QUALITY SYSTEMS, QUALITY CONTROL

EXPERIENCE PREFERRED

  • Knowledge and experience with QMS principles and ISO 9001.
  • Relevant Quality professional qualification







PRIMARY ROLE RESPONSIBILITIES

Quality Management System

  • Own, maintain, and continuously improve the site Quality Management System in accordance with ISO 9001 and applicable customer/industry standards.
  • Serve as the Management Representative for quality at the Chicopee facility; coordinate internal and external quality audits and management reviews.
  • Develop, issue, and maintain controlled quality documentation: work instructions, inspection plans, standard operating procedures, and quality records.
  • Establish and monitor key quality performance indicators (KPIs), report results to the site leadership on a regular cadence.
  • Drive corrective and preventive action (CAPA) processes, ensuring root-cause analysis is thorough and effective actions are implemented and verified.
  • Manage the calibration program for all measuring and test equipment on site.


QC Team Leadership & Inspection Operations

  • Directly supervise the site QC team; schedule workload to support production priorities and on-time delivery.
  • Provide technical direction on inspection methods, measurement techniques, GD&T interpretation, and use of precision measurement equipment (CMM, profilometers, hardness testers, etc.).
  • Oversee first article, in-process, and final inspection activities for precision-machined turbomachinery components (impellers, seals, sleeves, casings, shafts, and related parts).
  • Review and approve inspection reports, first article inspection reports (FAIRs), and material certifications; ensure documentation is complete and traceable before components are released.
  • Lead the nonconformance (NC) disposition process: facilitate MRB reviews, issue NCRs, coordinate rework/repair, and track closure.
  • Train and mentor QC personnel on inspection practices, quality standards, and RMS procedures; identify skills gaps and arrange targeted development.


Production & Engineering Collaboration

  • Partner with the Shop Supervision and machinists to resolve quality issues at the source and prevent recurrence; support setup approvals and first-off inspections.
  • Review customer drawings, specifications, and contract quality requirements; translate these into inspection plans and traveler hold-points prior to job release.
  • Collaborate with Engineering to evaluate design-for-manufacturability, identify inspection risk areas, and align on acceptable tolerance interpretation.
  • Participate in project kick-off meetings and work order reviews to identify quality requirements, witness/hold points, and customer-specific needs.
  • Support process qualification activities, including review of special process approvals (heat treatment, NDE, coatings) as they relate to component acceptance.


Supplier & Customer Quality

  • Support incoming inspection of purchased materials, raw stock, and subcontracted components; coordinate with purchasing to address supplier nonconformances.
  • Participate in supplier evaluations and audits; maintain records of supplier performance and escalate repeat issues through the CAPA process.
  • Serve as the primary quality point of contact for customer quality representatives, third-party inspectors, and regulatory/certification auditors during shop visits.
  • Respond to customer quality escapes and field complaints: coordinate investigations, prepare formal responses, and communicate resolution timelines.


ADDITIONAL RESPONSIBILITIES

Key Success Factors:

  • Perceptible culture of Quality
  • Quality costs aligned with business goals.
  • Continued ISO-9001 accreditation.
  • Willingness to “roll-up sleeves” to get the job done vs. delegating up or down the organization.


General:

The above list of activities is not all-inclusive but rather a general representation of the RMS Quality Manager's requirements. The above list is subject to change based on the company's needs.


REQUIRED EXPERIENCE & QUALIFICATIONS
  • Minimum 7 years of quality assurance/control experience in precision machining, aerospace, power generation, or rotating equipment manufacturing environment.
  • Demonstrated experience leading a QC team and managing a Quality Management System in a job-shop or low-volume, high-complexity production environment.
  • Hands-on experience with CMM operation, precision measurement instruments, and inspection of close-tolerance machined components.
  • Strong background in nonconformance management, root-cause analysis, and corrective/preventive action (CAPA).
  • Familiarity with turbomachinery components and the associated design, manufacturing, and inspection requirements is strongly preferred.


REQUIRED EDUCATION
  • Bachelor’s degree in Engineering, Manufacturing Technology, Materials Science, or a closely related technical discipline required.
  • Equivalent combination of technical education and directly applicable manufacturing quality experience will be considered.


ADDITIONAL REQUIREMENTS

Technical Knowledge

  • Expert-level ability to read and interpret engineering drawings, including GD&T per ASME Y14.5.
  • Working knowledge of ISO 9001 requirements; experience as a management system owner or internal/lead auditor.
  • Familiarity with NDE methods (MT, PT, UT, RT) and special processes (heat treatment, coatings) as they apply to component acceptance.
  • Proficiency in Microsoft Office; experience with ERP/MRP systems and QMS software.

Certifications (Preferred)

  • ASQ Certified Quality Engineer (CQE), Certified Quality Manager/OE (CMQ/OE), or equivalent.
  • ISO 9001 Lead Auditor certification.

Work Environment


  • While performing the duties of this position, the employee may work/enter a shop environment with exposure to moving mechanical parts. While the work area may be described as generally clean, safe, and "not loud", there will be machining operations that generate moderate noise.