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Contract Development Jobs in Massachusetts (NOW HIRING)

Danaher

Business Development Manager

Boston, MA · On-site

$145K - $175K/yr

At least 1 year of sales experience for Contract Development and/or Contract manufacturing Organizations supporting Cell and Gene Therapies, or equivalent experience. * At least 1 year of sales ...

Danaher

Business Development Manager

Boston, MA · On-site +1

$145K - $175K/yr

At least 1 year of sales experience for Contract Development and/or Contract manufacturing Organizations supporting Cell and Gene Therapies, or equivalent experience. * At least 1 year of sales ...

Biogen

Senior Engineer II, Device Development

Cambridge, MA · Hybrid

$114K - $156K/yr

Oversee verification activities at contract laboratories by developing experimental plans ... Experience with research and development of electromechanical medical devices, handheld delivery ...

Biogen

Senior Engineer II, Device Development

Cambridge, MA · On-site

$114K - $156K/yr

Oversee verification activities at contract laboratories by developing experimental plans ... Experience with research and development of electromechanical medical devices, handheld delivery ...

Ocean Spray

Attorney

Middleborough, MA · On-site

$125 - $150/hr

Your focus will be on supporting litigation activity, commercial contract development, and managing legal risks. You will work closely with internal teams to provide strategic legal advice that ...

Ocean Spray

Attorney

Lakeville, MA · On-site +1

$116K - $145K/yr

Your focus will be on supporting litigation activity, commercial contract development, and managing legal risks. You will work closely with internal teams to provide strategic legal advice that ...

Ocean Spray

Attorney

Lakeville, MA · On-site +1

$116K - $145K/yr

Your focus will be on supporting litigation activity, commercial contract development, and managing legal risks. You will work closely with internal teams to provide strategic legal advice that ...

Ocean Spray

Attorney

Lakeville, MA · On-site

$116K - $145K/yr

Your focus will be on supporting litigation activity, commercial contract development, and managing legal risks. You will work closely with internal teams to provide strategic legal advice that ...

Ocean Spray Cranberries

Attorney

Lakeville, MA · On-site +1

$116K - $145K/yr

Your focus will be on supporting litigation activity, commercial contract development, and managing legal risks. You will work closely with internal teams to provide strategic legal advice that ...

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Showing results 21-40

All JobsContract Development JobsContract Development Jobs in Massachusetts

Contract Development information

What is contract development?

Contract development refers to the process of creating, negotiating, and finalizing legal agreements between two or more parties. Professionals in contract development ensure that all terms, conditions, and obligations are clearly defined and legally enforceable. This role often involves collaborating with legal, procurement, and business teams to protect organizational interests and minimize risks. Effective contract development is crucial for successful partnerships and compliance with laws and regulations.

What are the key skills and qualifications needed to thrive in contract development, and why are they important?

To excel in Contract Development, you need expertise in contract law, negotiation, and drafting, often supported by a degree in law, business, or a related field. Familiarity with contract management systems, legal research tools, and compliance software is typically required. Strong attention to detail, analytical thinking, and effective communication help professionals craft clear agreements and manage stakeholder relationships. These skills and qualities are crucial for minimizing risk, ensuring legal compliance, and supporting successful business outcomes.

What are some common challenges faced in a contract development role, and how can they be managed effectively?

Professionals in Contract Development often encounter challenges such as negotiating complex terms, ensuring compliance with changing regulations, and balancing the needs of multiple stakeholders. Successfully managing these issues requires strong communication skills, attention to detail, and the ability to stay organized under tight deadlines. Building collaborative relationships with legal, procurement, and business teams is also essential for resolving ambiguities and achieving mutually beneficial agreements.

What is the difference between Contract Development vs Contract Manufacturing?

AspectContract DevelopmentContract Manufacturing
Primary FocusDesigning and developing new products or formulationsProducing and manufacturing products based on existing designs
Required SkillsResearch, formulation, regulatory knowledgeProduction processes, quality control, equipment operation
Work EnvironmentLaboratories, R&D facilitiesManufacturing plants, production lines
Industry UsagePharmaceuticals, biotech, consumer goodsPharmaceuticals, chemicals, food industries

Contract Development involves creating new products and formulations, focusing on research and design. In contrast, Contract Manufacturing centers on producing these products at scale, emphasizing manufacturing processes and quality control. Both roles are essential in bringing products from concept to market, but they differ in scope and daily activities.

What does a contract development do?

A contract development professional is responsible for creating, negotiating, and managing contracts between organizations and clients or vendors. They ensure that contractual terms comply with legal standards and organizational policies, often working closely with legal teams and using contract management tools. Their work helps mitigate risks and ensures clear agreements are in place for business operations.

What are the most commonly searched types of Development jobs in Massachusetts?

The most popular types of Development jobs in Massachusetts are:

Contract Development jobs near you
Infographic showing various Contract Development job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution.

Scientist, Quality Control Analytical Development (6-month Contract)

Rentschler

Milford, MA • On-site

$45 - $55/hr

Full-time

This job post has expired 3 days ago. Applications are no longer accepted.

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.
Duties and Responsibilities
  • Laboratory role to support the qualification and validation of analytical methods for biologic drugs and process related impurities
  • Primary focus on the execution of experiments to support the validation of molecular biology assays including but not limited to ELISAs for residual HCP, residual protein a, and relative potency assays as well as qPCR
  • Work collaboratively within a group of scientists to perform analytical method development qualification or validation under cGMP in collaboration with the Quality Control unit
  • Apply expertise in molecular biology, cell biology and/or immunochemistry to analytical development team across the lifecycle of the procedures
  • Participate in the technology transfer of analytical methods into QC and analytical method qualification Method transfer, method validation, method development
  • Review & revise SOPs and/or author reports, protocols & other documentation as appropriate
  • Collaborate with other labs to prepare methods for transfer to the QC GMP labs
  • Provide training and work direction for group members as required

Qualifications
  • Bachelor's Degree in chemistry or a biological science with minimum of
  • 5+ years of related experience (or master's degree with 2+ years of experience) in a cGMP environment
  • Experience utilizing Spectramax M5 or M2 plate readers and the associated Softmax GMP software required
  • Strong understanding of molecular biology assays in support of the product quality testing for Biologics drug substances/drug products
  • Experience with analytical characterization of biologics is expected
  • Strong organizational, time management skills, and prioritize work schedule to meet deadlines
  • Must be able to communicate effectively with managers, peers, and clients
  • Must demonstrate effectiveness in ability to train others as needed
  • Strong knowledge and expertise of quality requirements pertinent to pharmaceutical AD labs
  • Strong working knowledge of laboratory safety including standard precautions associated with
  • hazardous & biohazardous material handling
  • Experience with drug substance, drug products, intermediates, as well as experience with monoclonal antibodies is desired
  • Experience in other biophysical characterization methods CE (capillary electrophoresis), chromatography, SEC/RP/IEX-U(H)PLC, SDS-CGE, iCIEF, CIEX, Peptide mapping is a plus
  • Computer skills to include full competence with Microsoft Word, Power Point & Excel

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

Physical Requirements
  • Frequent lifting up to 10 lbs.; frequent standing/walking
  • Manual and visual dexterity required to perform laboratory and computer tasks for prolonged periods
  • PPE as required

Base Pay Range
$45/hr - $55/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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