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Stability Manager Jobs in Massachusetts (NOW HIRING)

Stability Healthcare

Travel RN Home Health

Salem, MA · On-site

Stability Healthcare is seeking a travel nurse RN Case Manager, Home Health for a travel nursing job in Salem, Massachusetts. & Requirements * Specialty: Home Health * Discipline: RN * Duration: 13 ...

Stability Healthcare

Travel RN Home Health

Salem, MA · On-site

Stability Healthcare is seeking a travel nurse RN Case Manager, Home Health for a travel nursing job in Salem, Massachusetts. & Requirements * Specialty: Home Health * Discipline: RN * Duration: 13 ...

Stability Healthcare

Travel Home Health RN

Salem, MA · On-site

Stability Healthcare is seeking a travel nurse RN Home Health for a travel nursing job in Salem ... The ability to manage time and tasks are critical skills needed for these positions. While this ...

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Stability Manager information

What is a stability manager?

Stability Managers are professionals responsible for ensuring the consistent quality, safety, and efficacy of products over time, particularly in industries like pharmaceuticals, biotechnology, or food production. They design and oversee stability studies, analyze data, and ensure compliance with regulatory standards. Their work helps companies guarantee that products remain effective and safe throughout their shelf life, supporting both regulatory approval and customer satisfaction.

What skills and qualifications are needed to be a stability manager?

To thrive as a Stability Manager, you need expertise in quality assurance, regulatory compliance, data analysis, and a background in pharmaceutical sciences or a related field. Familiarity with stability testing protocols, LIMS (Laboratory Information Management Systems), and ICH guidelines, as well as experience with relevant certifications such as GMP, is typically required. Strong organizational, problem-solving, and communication skills help manage cross-functional teams and ensure timely project delivery. These skills are crucial for ensuring product quality, regulatory compliance, and the successful management of stability programs in the pharmaceutical industry.

How does a stability manager collaborate with cross-functional teams during product development?

A Stability Manager works closely with departments such as R&D, Quality Assurance, Regulatory Affairs, and Manufacturing to ensure that products meet stability requirements throughout development and after launch. They coordinate stability studies, communicate testing schedules, and interpret data to inform formulation or packaging adjustments. Regular meetings and clear documentation are essential for aligning on regulatory guidelines and resolving any issues that arise, making strong communication and teamwork vital to success in this role.

What is the difference between Stability Manager vs Maintenance Supervisor?

AspectStability ManagerMaintenance Supervisor
CredentialsTypically requires a degree in engineering or related field, with certifications in safety or project managementUsually requires a high school diploma or technical training, with certifications in safety and equipment operation
Work EnvironmentOversees stability and safety protocols in industrial or manufacturing settingsManages maintenance teams and schedules repairs in similar environments
Employer & Industry UsageCommonly employed in manufacturing, chemical, or energy sectorsFound in manufacturing, facilities management, and industrial plants

The Stability Manager focuses on ensuring the safety and stability of processes and structures, often overseeing safety protocols and risk assessments. In contrast, the Maintenance Supervisor manages equipment maintenance and repairs. Both roles are vital in industrial settings, but the Stability Manager emphasizes safety and process stability, while the Maintenance Supervisor concentrates on operational upkeep.

What are popular job titles related to Stability Manager jobs in Massachusetts?

For Stability Manager jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Stability Manager jobs in Massachusetts look for?

The top searched job categories for Stability Manager jobs in Massachusetts are:

What cities in Massachusetts are hiring for Stability Manager jobs?

Cities in Massachusetts with the most Stability Manager job openings:

Stability Manager jobs near you
Infographic showing various Stability Manager job openings in Massachusetts as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Quality Control Analyst II, Release & Stability Testing (3rd Shift - Contract)

Rentschler

Milford, MA • On-site

$39 - $46/hr

Full-time

Posted 22 days ago

Job description

Advancing medicine to save lives. Together.
Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially for patients with rare and serious diseases.
Rentschler Biopharma SE is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. We offer customized full-service solutions for bioprocess development and the production of complex biopharmaceuticals. As a German family-owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best-in-class solutions - together with our clients.
Rentschler Biopharma has approximately 1,400 employees and is headquartered in Laupheim, Germany, with a site in Milford, MA, USA. In 2024, we joined the United Nations Global Compact, underlining our commitment to sustainability.
As an independent family-owned company, we live by the motto: Many hands, many minds - ONE TEAM! Open, respectful cooperation characterizes our working environment, where quality awareness, diligence and responsibility are our top priorities. With all the diversity of our talents in the Rentschler team, we pursue one vision together: advancing medicine to save lives.
The Quality Control Analyst II, Release and Stability Testing is responsible for the cGMP analytical testing of stability samples and evaluation of data to ensure compliance with analytical methods, stability protocols, client criteria, Good Laboratory Practices (GLP) and Good Manufacturing Practices (cGMP). They work independently with minimal supervision ensuring stability tests are performed promptly within predefined testing windows. The Quality Control Analyst II, Release and Stability Testing, ensures all work performed strictly adheres to cGMP, SOPs, and protocols. They collaborate with QC team members and cross functional teams for timely resolution of quality issues to achieve project goals. They are responsible for identifying and resolving problems of diverse scope in which analysis of data requires evaluation of identifiable factors based on biochemical knowledge and background.
Join our QC team with a quality mindset first to help make and release medicines for better lives. Our team is built on trust, respect, and integrity. The quality mindset is about operating with reliability, efficiency, and honest feedback.
Duties and Responsibilities
  • Perform analytical testing using HPLC/UPLC/cGE/icIEF instruments following GMP documents
  • Create/revise SOPs, Protocols and Reports
  • Practice safe work habits and adhere to safety procedures and guidelines
  • Perform maintenance and cleaning of laboratory equipment
  • SME to support or lead activities related to OOS/OOT investigations, deviations, change controls, corrective actions, and preventive actions to correct and eliminate the potential for non-conformances
  • Update and track metrics for trending and reporting; stability and QC analytical data
  • Task and team-oriented, analytical, organized, detail-oriented, self-motivated and ability to multitask
  • Proficient with MS Outlook, Word, Excel and PowerPoint, and other electronic systems
  • Exceptional communication and interpersonal skills
  • Assists in training of new hires and retraining of QC laboratory staff, as needed
  • Performs other duties as assigned

Qualifications
  • Bachelor's Degree in Life Sciences discipline
  • Minimum 3+ years' experience in a cGMP analytical lab environment
  • Must have the ability and skill to perform the detailed job requirements competently, safely, accurately, and proficiently
  • Self-starting motivated person who possesses excellent time management, the ability to adapt to change and organizational skills
  • Able to communicate, receive, and understand information and ideas with diverse groups of people in a collaborative, comprehensible and reasonable manner
  • Able to use and learn standard office equipment and technology with proficiency
  • Experience in Empower chromatography software

Working Conditions
  • Laboratory environment working with chemical reagents and analytical equipment
  • Normal office working conditions: computer, phone, files, fax, copier
  • Personal Protective Equipment must be worn as required
  • Minimum travel required
  • Work is to be performed on site
  • Possible weekend/off hours testing may be required

Physical Requirements
  • Frequent standing/walking
  • PPE as required
  • Able to work upright and stationary and/or standing for typical working hours
  • Able to lift and move objects up to 25 pounds

Base Pay Range
$39/hr - $46/hr
Disclosure Statement
Rentschler Biopharma, Inc is committed to fair and equitable compensation practices. The base pay range listed for this position is the anticipated annual base salary range the organization reasonably, and in good faith, expects to pay for this position at this time. Actual compensation is determined based on several factors that may include seniority, education, training, relevant experience, relevant certifications, geography of work location, job responsibilities, or other application factors permissible by law. The salary pay range is subject to change and may be modified at any time.

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