... support projects in the portfolio pipeline. Responsibilities include wet lab support using ... Additional duties involve interfacing with the external inventory management organization to ...
Quick apply
... support projects in the portfolio pipeline. Responsibilities include wet lab support using ... Additional duties involve interfacing with the external inventory management organization to ...
Senior Mechanical Engineer - Utilities & Environmental Systems
Andover, MA · On-site
$99K - $165K/yr
You will manage projects by meeting objectives and preparing forecasts for resource requirements ... Design and support HVAC and utility systems for pharmaceutical, biotech, manufacturing, and ...
Senior Mechanical Engineer - Utilities & Environmental Systems
Andover, MA · On-site
$99K - $165K/yr
You will manage projects by meeting objectives and preparing forecasts for resource requirements ... Design and support HVAC and utility systems for pharmaceutical, biotech, manufacturing, and ...
... project planning and execution phases, and provide budgeting/financial flexibility by offering ... biotech production or R&D experience, and/or pharmaceutical regulatory submission writing ...
... project planning and execution phases, and provide budgeting/financial flexibility by offering ... biotech production or R&D experience, and/or pharmaceutical regulatory submission writing ...
... biotech, and industrial customers. Working closely with sales teams and customers, you'll deliver ... project management and organizational capabilities • Ability to travel 50-75% of time to customer ...
... biotech, and industrial customers. Working closely with sales teams and customers, you'll deliver ... project management and organizational capabilities • Ability to travel 50-75% of time to customer ...
... managing people and or leadership experience leading teams, project, programs or directing the allocation of resources * Clinical/medical research experience * 6 years of experience in a biotech ...
... managing people and or leadership experience leading teams, project, programs or directing the allocation of resources * Clinical/medical research experience * 6 years of experience in a biotech ...
Director, Validation
Bedford, NH · On-site
... or Biotechnology industry, required. * Sound industry knowledge of pharmaceutical and medical ... Strong experience with project and people management, particularly for large validation projects or ...
Director, Validation
Bedford, NH · On-site
... or Biotechnology industry, required. * Sound industry knowledge of pharmaceutical and medical ... Strong experience with project and people management, particularly for large validation projects or ...
Director, Validation
Bedford, NH · On-site
... or Biotechnology industry, required. * Sound industry knowledge of pharmaceutical and medical ... Strong experience with project and people management, particularly for large validation projects or ...
Director, Validation
Bedford, NH · On-site
... or Biotechnology industry, required. * Sound industry knowledge of pharmaceutical and medical ... Strong experience with project and people management, particularly for large validation projects or ...
... manage complex projects and influence stakeholders across functions i.e. Finance, HR and IT ... Preferred : • Experience in the medical device, biotech, or pharmaceutical industry preferred ...
... manage complex projects and influence stakeholders across functions i.e. Finance, HR and IT ... Preferred : • Experience in the medical device, biotech, or pharmaceutical industry preferred ...
Manage small-scale projects such as system upgrades, patching cycles, or equipment integrations ... biotech, or medical device environment. * Strong computer proficiency, including: * Checking and ...
Manage small-scale projects such as system upgrades, patching cycles, or equipment integrations ... biotech, or medical device environment. * Strong computer proficiency, including: * Checking and ...
Manage smallscale projects such as system upgrades, patching cycles, or equipment integrations ... biotech, or medical device environment. * Strong computer proficiency, including: * Checking and ...
Manage smallscale projects such as system upgrades, patching cycles, or equipment integrations ... biotech, or medical device environment. * Strong computer proficiency, including: * Checking and ...
Support and Perform Lot Disposition for Biotech semi-finished and finished products (if applicable ... Demonstrated ability to manage multiple projects and priorities. Demonstrated ability to prioritize ...
Quick apply
Support and Perform Lot Disposition for Biotech semi-finished and finished products (if applicable ... Demonstrated ability to manage multiple projects and priorities. Demonstrated ability to prioritize ...
Support and Perform Lot Disposition for Biotech semi-finished and finished products (if applicable ... manage multiple projects and priorities Demonstrated ability to prioritize work, to act and work ...
Quick apply
Support and Perform Lot Disposition for Biotech semi-finished and finished products (if applicable ... manage multiple projects and priorities Demonstrated ability to prioritize work, to act and work ...
Proven ability to manage complex projects and influence stakeholders across functions i.e. Finance ... Experience in the medical device, biotech, or pharmaceutical industry preferred. * Workday ...
Proven ability to manage complex projects and influence stakeholders across functions i.e. Finance ... Experience in the medical device, biotech, or pharmaceutical industry preferred. * Workday ...
No The individual will manage, coordinate, and maintain cGMP documentation, procedures, and records ... Lead continuous improvement efforts and projects across the department, or multiple departments.
No The individual will manage, coordinate, and maintain cGMP documentation, procedures, and records ... Lead continuous improvement efforts and projects across the department, or multiple departments.
Proven ability to manage complex projects and influence stakeholders across functions i.e. Finance ... Experience in the medical device, biotech, or pharmaceutical industry preferred. * Workday ...
Proven ability to manage complex projects and influence stakeholders across functions i.e. Finance ... Experience in the medical device, biotech, or pharmaceutical industry preferred. * Workday ...
No The individual will manage, coordinate, and maintain cGMP documentation, procedures, and records ... Lead continuous improvement efforts and projects across the department, or multiple departments.
No The individual will manage, coordinate, and maintain cGMP documentation, procedures, and records ... Lead continuous improvement efforts and projects across the department, or multiple departments.
Accounts Receivable Collections Specialist
Andover, MA · On-site
$65K - $85K/yr
What You'll Do: • Manage accounts receivable aging and proactively follow up on outstanding ... special projects and reporting as needed. • Maintain professionalism and excellent customer ...
Accounts Receivable Collections Specialist
Andover, MA · On-site
$65K - $85K/yr
What You'll Do: • Manage accounts receivable aging and proactively follow up on outstanding ... special projects and reporting as needed. • Maintain professionalism and excellent customer ...
Qa Specialist Ii - Ops
Bedford, NH · On-site
Lead improvement projects and communicate status to management * Serve as QA representative to ... biotech industry experience with 3+ years of experience in a QA Operations role supporting late ...
Qa Specialist Ii - Ops
Bedford, NH · On-site
Lead improvement projects and communicate status to management * Serve as QA representative to ... biotech industry experience with 3+ years of experience in a QA Operations role supporting late ...
Qa Specialist Ii - Ops
Bedford, NH · On-site
Lead improvement projects and communicate status to management * Serve as QA representative to ... biotech industry experience with 3+ years of experience in a QA Operations role supporting late ...
Qa Specialist Ii - Ops
Bedford, NH · On-site
Lead improvement projects and communicate status to management * Serve as QA representative to ... biotech industry experience with 3+ years of experience in a QA Operations role supporting late ...
QA Specialist II - Operations
Bedford, NH · On-site
Lead improvement projects and communicate status to management * Serve as QA representative to ... biotech industry experience with 3+ years of experience in a QA Operations role supporting late ...
QA Specialist II - Operations
Bedford, NH · On-site
Lead improvement projects and communicate status to management * Serve as QA representative to ... biotech industry experience with 3+ years of experience in a QA Operations role supporting late ...
Project Manager Biotech information
See Manchester, NH salary details
$21.34 - $26.17
4% of jobs
$26.17 - $31.01
8% of jobs
$31.01 - $35.85
3% of jobs
$37.97 is the 25th percentile. Wages below this are outliers.
$35.85 - $40.69
21% of jobs
The median wage is $43.71 / hr.
$40.69 - $45.53
21% of jobs
$48.80 is the 75th percentile. Wages above this are outliers.
$45.53 - $50.37
25% of jobs
$50.37 - $55.20
13% of jobs
$55.20 - $60.04
2% of jobs
$60.04 - $64.88
1% of jobs
$64.88 - $69.72
1% of jobs
$69.72 - $74.56
0% of jobs
$21
$45
$74
How much do project manager biotech jobs pay per hour?
As of Aug 17, 2026, the average hourly pay for project manager biotech in Manchester, NH is $45.10, according to ZipRecruiter salary data. Most workers in this role earn between $39.13 and $49.47 per hour, depending on experience, location, and employer.
What is the difference between Project Manager Biotech vs Clinical Project Manager?
| Aspect | Project Manager Biotech | Clinical Project Manager |
|---|---|---|
| Credentials | Bachelor's or Master's in Life Sciences, Project Management Certification | Bachelor's or Master's in Life Sciences, Clinical Research Certification |
| Work Environment | Biotech companies, R&D labs, manufacturing | Clinical trial sites, hospitals, pharmaceutical companies |
| Industry Usage | Biotech product development, research projects | Clinical trial management, regulatory compliance |
| Common Search/Comparison | Yes | Yes |
The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.
How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?
A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.
What does a project manager in biotech do?
A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.
What are the key skills and qualifications needed to thrive as a project manager in biotech?
To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.
What are popular job titles related to Project Manager Biotech jobs in Manchester, NH?
For Project Manager Biotech jobs in Manchester, NH, the most frequently searched job titles are:
What job categories do people searching Project Manager Biotech jobs in Manchester, NH look for?
The top searched job categories for Project Manager Biotech jobs in Manchester, NH are:
What cities near Manchester, NH are hiring for Project Manager Biotech jobs?
Cities near Manchester, NH with the most Project Manager Biotech job openings:
Contractor
Re-posted 29 days ago
Job description
Position Details:
Our client, a world-leading Pharmaceutical Company in Andover, MA is currently looking for an Scientist I to join their expanding team.
Job Title: Scientist I / Protein Characterization
Duration: 12 months contract, extendable up to 48 months
Location: Andover, MA
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Our client, a world-leading Pharmaceutical Company in Andover, MA is currently looking for an Scientist I to join their expanding team.
Job Title: Scientist I / Protein Characterization
Duration: 12 months contract, extendable up to 48 months
Location: Andover, MA
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
The successful candidate will join the Critical Reagents group to support projects in the portfolio pipeline.
Responsibilities include wet lab support using characterization techniques and generation of critical reagent conjugates.
Additional duties involve interfacing with the external inventory management organization to integrate information and knowledge of critical reagents, registration and submission into the centralized inventory for life cycle inventory and resupply purposes.
The incumbent will assist with lab operations through activities such as the generation and tracking of purchase orders and costs, buffer supplies, organization of freezers, and uploading and managing critical reagent characterization summaries on local internet sites.
The incumbent should have 0-3 years of experience in the biotechnology or pharmaceutical industry.
The incumbent should have 0-3 years of experience in the biotechnology or pharmaceutical industry.
Most Critical Skills Needed:
A Bachelor's degree in biology, biochemistry or related field is required.
Knowledge of protein characterization techniques such as ligand binding assays (ELISA), BCA, SDS-PAGE, Western blot, Octet, UV Vis, and analytical SEC is a plus.
Ability to excel in a collaborative, fast paced and dynamic environment is essential.
Excellent organizational and communication skills.
A flexible approach and team-oriented work style will be critical to the success of the candidate.
Good critical and strategic thinking, logical thought process, willingness to learn, troubleshoot and resolve issues and work across multiple disciplinary groups.
Proficiency in Microsoft Office software suite.