Leverage strong technical writing capabilities to independently author and initiate deviation ... Ready to shape the future of life sciences? Apply now.
Leverage strong technical writing capabilities to independently author and initiate deviation ... Ready to shape the future of life sciences? Apply now.
Bachelor's degree in a scientific, engineering, manufacturing, or related field preferred * 3-5 ... Strong technical writing, organizational, and problem-solving skills * Strong communication and ...
Bachelor's degree in a scientific, engineering, manufacturing, or related field preferred * 3-5 ... Strong technical writing, organizational, and problem-solving skills * Strong communication and ...
Bachelor's degree in a scientific, engineering, manufacturing, or related field preferred * 3-5 ... Strong technical writing, organizational, and problem-solving skills * Strong communication and ...
Bachelor's degree in a scientific, engineering, manufacturing, or related field preferred * 3-5 ... Strong technical writing, organizational, and problem-solving skills * Strong communication and ...
Exceptional technical writing skills and the ability to present complex scientific data clearly to senior management and auditors. About Lonza At Lonza, our people are our greatest strength. With 30 ...
Exceptional technical writing skills and the ability to present complex scientific data clearly to senior management and auditors. About Lonza At Lonza, our people are our greatest strength. With 30 ...
Exceptional technical writing skills and the ability to present complex scientific data clearly to senior management and auditors. About Lonza At Lonza, our people are our greatest strength. With 30 ...
Exceptional technical writing skills and the ability to present complex scientific data clearly to senior management and auditors. About Lonza At Lonza, our people are our greatest strength. With 30 ...
... technical writing. * Promote housekeeping, 6S, daily management practices, and continuous improvement. What we are looking for: * AS or BS degree in a science-related field; a high school diploma ...
... technical writing. * Promote housekeeping, 6S, daily management practices, and continuous improvement. What we are looking for: * AS or BS degree in a science-related field; a high school diploma ...
Writes technical procedures utilizing the CLSI format. Performs supervisory responsibilities in ... Volunteers for additional tasks. * Demonstrates compliance with corporate, departmental and job ...
Writes technical procedures utilizing the CLSI format. Performs supervisory responsibilities in ... Volunteers for additional tasks. * Demonstrates compliance with corporate, departmental and job ...
Writes technical procedures utilizing the CLSI format. Performs supervisory responsibilities in ... Volunteers for additional tasks. * Demonstrates compliance with corporate, departmental and job ...
Writes technical procedures utilizing the CLSI format. Performs supervisory responsibilities in ... Volunteers for additional tasks. * Demonstrates compliance with corporate, departmental and job ...
Medical Laboratory Scientist II - FT/Nights
Dover, NH · On-site
$30.50 - $48.10/hr
... consultant, technical supervisor, clinical consultant, or Laboratory Director. Document all ... written protocols, including communication with supervisors when issues are identified. - Must be ...
New
Medical Laboratory Scientist II - FT/Nights
Dover, NH · On-site
$30.50 - $48.10/hr
... consultant, technical supervisor, clinical consultant, or Laboratory Director. Document all ... written protocols, including communication with supervisors when issues are identified. - Must be ...
New
1463 Senior QA Compliance Specialist
Portsmouth, NH · On-site
$69 - $79.58/hr
Bachelor's degree in life sciences or equivalent experience. * Preferred: Master's degree or ... Languages * English (business fluent -- written and spoken). Required Skills & Competencies
Quick apply
1463 Senior QA Compliance Specialist
Portsmouth, NH · On-site
$69 - $79.58/hr
Bachelor's degree in life sciences or equivalent experience. * Preferred: Master's degree or ... Languages * English (business fluent -- written and spoken). Required Skills & Competencies
Biotechnologist III (Days)
Portsmouth, NH · On-site
... technical writing * Attention to detail with strong problem-solving and decision-making skills * High school diploma or equivalent required; Associate's or Bachelor's degree in a science-related ...
Biotechnologist III (Days)
Portsmouth, NH · On-site
... technical writing * Attention to detail with strong problem-solving and decision-making skills * High school diploma or equivalent required; Associate's or Bachelor's degree in a science-related ...
... technical writing * Attention to detail with strong problem-solving and decision-making skills * High school diploma or equivalent required; Associate's or Bachelor's degree in a science-related ...
... technical writing * Attention to detail with strong problem-solving and decision-making skills * High school diploma or equivalent required; Associate's or Bachelor's degree in a science-related ...
Our North Atlantic Operations is a multi-disciplinary environmental, science, architecture, and ... Effective technical, written, and verbal communication skills Preferred Qualifications: * NH ...
Our North Atlantic Operations is a multi-disciplinary environmental, science, architecture, and ... Effective technical, written, and verbal communication skills Preferred Qualifications: * NH ...
Biotechnologist III (Days)
Portsmouth, NH · On-site
... technical writing * Attention to detail with strong problem-solving and decision-making skills * High school diploma or equivalent required; Associate's or Bachelor's degree in a science-related ...
Biotechnologist III (Days)
Portsmouth, NH · On-site
... technical writing * Attention to detail with strong problem-solving and decision-making skills * High school diploma or equivalent required; Associate's or Bachelor's degree in a science-related ...
... technical writing * Attention to detail with strong problem-solving and decision-making skills * High school diploma or equivalent required; Associate's or Bachelor's degree in a science-related ...
... technical writing * Attention to detail with strong problem-solving and decision-making skills * High school diploma or equivalent required; Associate's or Bachelor's degree in a science-related ...
Intern, CMC Development (Summer 2027)
Rochester, NH · On-site
$20 - $60/hr
Use laboratory, technical and communication skills to generate experimental results, perform data ... Strong fundamental scientific and engineering skills for the evaluation of experimental data
New
Intern, CMC Development (Summer 2027)
Rochester, NH · On-site
$20 - $60/hr
Use laboratory, technical and communication skills to generate experimental results, perform data ... Strong fundamental scientific and engineering skills for the evaluation of experimental data
New
Intern, CMC Development (Summer 2027)
Derry, NH · On-site
$20 - $60/hr
Use laboratory, technical and communication skills to generate experimental results, perform data ... Strong fundamental scientific and engineering skills for the evaluation of experimental data
New
Intern, CMC Development (Summer 2027)
Derry, NH · On-site
$20 - $60/hr
Use laboratory, technical and communication skills to generate experimental results, perform data ... Strong fundamental scientific and engineering skills for the evaluation of experimental data
New
... technical writing * Attention to detail with strong problem-solving and decision-making skills * High school diploma or equivalent required; Associate's or Bachelor's degree in a science-related ...
... technical writing * Attention to detail with strong problem-solving and decision-making skills * High school diploma or equivalent required; Associate's or Bachelor's degree in a science-related ...
Intern, CMC Development (Summer 2027)
Concord, NH · On-site
$20 - $60/hr
Use laboratory, technical and communication skills to generate experimental results, perform data ... Strong fundamental scientific and engineering skills for the evaluation of experimental data
New
Intern, CMC Development (Summer 2027)
Concord, NH · On-site
$20 - $60/hr
Use laboratory, technical and communication skills to generate experimental results, perform data ... Strong fundamental scientific and engineering skills for the evaluation of experimental data
New
Intern, CMC Development (Summer 2027)
Rochester, NH · On-site +1
$20 - $60/hr
Use laboratory, technical and communication skills to generate experimental results, perform data ... Strong fundamental scientific and engineering skills for the evaluation of experimental data
New
Intern, CMC Development (Summer 2027)
Rochester, NH · On-site +1
$20 - $60/hr
Use laboratory, technical and communication skills to generate experimental results, perform data ... Strong fundamental scientific and engineering skills for the evaluation of experimental data
New
Volunteer Scientific Technical Writer information
See Rochester, NH salary details
$13.41 - $18.07
2% of jobs
$18.07 - $22.74
7% of jobs
$22.74 - $27.40
12% of jobs
$28.49 is the 25th percentile. Wages below this are outliers.
$27.40 - $32.06
16% of jobs
The median wage is $35.56 / hr.
$32.06 - $36.72
17% of jobs
$36.72 - $41.39
14% of jobs
$44.42 is the 75th percentile. Wages above this are outliers.
$41.39 - $46.05
11% of jobs
$46.05 - $50.71
10% of jobs
$50.71 - $55.37
5% of jobs
$55.37 - $60.04
3% of jobs
$60.04 - $64.70
3% of jobs
$13
$38
$64
How much do volunteer scientific technical writer jobs pay per hour?
As of Sep 3, 2026, the average hourly pay for volunteer scientific technical writer in Rochester, NH is $38.11, according to ZipRecruiter salary data. Most workers in this role earn between $28.22 and $46.11 per hour, depending on experience, location, and employer.
What does a volunteer scientific technical writer do?
A Volunteer Scientific Technical Writer is responsible for creating, editing, and managing scientific documents such as research papers, technical manuals, grant proposals, and educational materials. They often work with researchers, scientists, or organizations to translate complex scientific concepts into clear, accessible language for different audiences. These writers may also help ensure documents adhere to specific formatting and publication standards, and contribute to public outreach by making scientific information more understandable. The role is typically unpaid and serves to support scientific communication and outreach efforts.
How does a volunteer scientific technical writer typically collaborate with scientists and subject matter experts?
Volunteer Scientific Technical Writers frequently work closely with researchers, scientists, and subject matter experts to translate complex scientific information into clear, accessible documents. This collaboration often involves conducting interviews, attending team meetings, and reviewing technical materials to ensure accuracy and clarity. Building strong working relationships, asking clarifying questions, and maintaining open communication are essential for effectively capturing and conveying the intended message. These collaborations can occur remotely or on-site, depending on the organization, and often require adaptability and strong interpersonal skills.
What are the key skills and qualifications needed to thrive as a volunteer scientific technical writer, and why are they important?
To thrive as a Volunteer Scientific Technical Writer, you need a solid foundation in scientific concepts, strong writing abilities, and attention to detail, often supported by a degree in science or technical writing. Familiarity with document management systems, reference management tools, and formatting standards like APA or MLA is typically required. Excellent communication, collaboration, and the ability to convey complex information clearly are standout soft skills in this role. These skills are essential for producing accurate, accessible scientific documentation that supports research and outreach efforts.
Full-time
Medical, Dental, Vision, PTO
Re-posted 27 days ago
Lonza rating
8.3
Based on 42 frontline employees who took The Breakroom Quiz
24th of 86 rated pharmaceutical
Job description
Supervisor, Production Support - Large Scale Allogenic
Location: Portsmouth, NH, USA.
Schedule: Monday to Friday, 0800-1700
We are seeking a dedicated operational leader to join our manufacturing team in Portsmouth, NH, as the Supervisor, Production Support. In this role, you will coordinate safety, quality, and daily manufacturing operations under strict cGMP conditions to support the production of cell therapy products for LSA. Operating under general supervision, you will provide leadership and oversight to the production support team, managing all routine operational and administrative activities that occur within the team for cGMP Cell Therapy production, including real-time, floor-based oversight, directing a team of manufacturing associates to ensure that all materials are ready and available in manufacturing suites to allow right first time of the production schedule seamlessly while maintaining absolute inspection readiness. This role acts as a vital cross-functional anchor-collaborating across departments to troubleshoot technical anomalies, overseeing critical document reviews, and driving continuous training to ensure right-first-time compliance.
What will you get?
What you'll do:
What we're looking for:
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
Location: Portsmouth, NH, USA.
Schedule: Monday to Friday, 0800-1700
We are seeking a dedicated operational leader to join our manufacturing team in Portsmouth, NH, as the Supervisor, Production Support. In this role, you will coordinate safety, quality, and daily manufacturing operations under strict cGMP conditions to support the production of cell therapy products for LSA. Operating under general supervision, you will provide leadership and oversight to the production support team, managing all routine operational and administrative activities that occur within the team for cGMP Cell Therapy production, including real-time, floor-based oversight, directing a team of manufacturing associates to ensure that all materials are ready and available in manufacturing suites to allow right first time of the production schedule seamlessly while maintaining absolute inspection readiness. This role acts as a vital cross-functional anchor-collaborating across departments to troubleshoot technical anomalies, overseeing critical document reviews, and driving continuous training to ensure right-first-time compliance.
What will you get?
- An agile career and dynamic working culture
- An inclusive and ethical workplace
- Direct Leadership Impact: Mentor, guide, and champion the career development of a dedicated shift of manufacturing professionals.
- Advanced Bioprocessing Footprint: Lead complex, life-saving therapeutic protein production within a world-class cGMP cleanroom environment.
- Compensation programs that recognize high performance
- Medical, dental and vision insurance, as well as PTO and more
- Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits.
What you'll do:
- Daily Operations Coordination: Supervise the shift-ly safety, quality compliance, and managing throughput of production support areas, providing real-time assistance and technical troubleshooting on the floor.
- Production Schedule Delivery: Partner closely with cross-functional support departments to safely execute daily manufacturing targets and ensure on-time delivery of planned production milestones.
- Quality & GxP Compliance Assurance: Mentor staff to maintain full compliance with all cGMP and internal Quality System requirements, proactively fostering a continuous state of inspection readiness.
- Batch Record Review: Lead and ensure the timely, detailed completion of document reviews-including batch records, logbooks, and localized data entries-minimizing deviations to support rapid batch release.
- Team Development & Line Management: Educate, guide, and champion shift employees through structured 1-on-1 meetings, regular performance evaluations, and dedicated career progression mapping.
- Administrative Shift Ownership: Direct core shift administrative tasks, including managing shift-exchange handovers, assigning daily floor duties, coordinating team training matrices, and assisting with recruitment/onboarding.
- Technical Document Authorship: Leverage strong technical writing capabilities to independently author and initiate deviation records, update Standard Operating Procedures (SOPs), and draft operational protocols.
- Continuous Improvement Execution: Actively participate in site-wide continuous improvement (Lean/5S) initiatives to optimize floor workflows, reduce waste, and enhance suite safety parameters.
What we're looking for:
- Experience: Significant experience working within a regulated manufacturing setting, with a strong preference for biopharmaceutical or biotechnology cGMP cleanroom environments.
- Industry Track Record: Ideally, candidates will bring experience operating at a Manufacturing Associate/Technician Level III tier within biopharma, biotech, life science, or medical device industries. Previous experience in a supervisory or shift-lead capacity is highly preferred.
- Technical Context: Prior practical exposure to upstream manufacturing methodologies within the biotech or pharmaceutical sector is preferred but not required.
- Critical Thinking & Decisions: Validated logic, critical thinking, and decisive troubleshooting capabilities under tight production timelines.
- Communication & Resilience: Exceptional written and verbal communication skills; a flexible, "go-getter" attitude capable of shifting with business priorities and translating performance feedback into prompt action.
- Education: High School Diploma or equivalent experience is required; an Associate's Degree (AS) or Bachelor's Degree (BS) in a science-related discipline is preferred.
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
About Lonza
Sourced by ZipRecruiter
Industry
Biotechnology research and development and pharmaceutical and medicine manufacturing
Company size
10,000+ Employees
Headquarters location
Bern, KS, US