Current jobs related to Manufacturing Technical Writer - Frederick - Pyramid Consulting, Inc
-
Technical Writer
2 weeks ago
Frederick, Maryland, United States US Tech Solutions Full timeJob SummaryUS Tech Solutions is seeking a skilled Technical Writer to support our GMP upstream and downstream manufacturing process. The ideal candidate will have experience in biotechnology/pharmaceutical manufacturing, excellent written and verbal communication skills, and proficiency in MS Office.ResponsibilitiesDevelop and revise standard operating...
-
Technical Writer
4 weeks ago
Frederick, Maryland, United States GForce Life Sciences Full timeJob Title: Technical WriterThe Technical Writer is a crucial member of the GForce Life Sciences team, responsible for creating high-quality documentation that supports the company's GMP upstream and downstream manufacturing process.Key Responsibilities:Develop and maintain standard operating procedures (SOPs) for manufacturing processes and routine...
-
Technical Writer
2 months ago
Frederick, United States GForce Life Sciences Full timeJob Title: Technical WriterOnsite in Frederick, MDDuration: 12+ months Job Description: We’re looking for a Technical Writer to help create and update documentation for our biologics manufacturing processes. You’ll be involved in writing and revising standard operating procedures, batch records, and other key documents. Your role will also include...
-
Technical Writer
4 weeks ago
Frederick, United States GForce Life Sciences Full timeJob Title: Technical WriterOnsite in Frederick, MDDuration: 12+ months Job Description: We’re looking for a Technical Writer to help create and update documentation for our biologics manufacturing processes. You’ll be involved in writing and revising standard operating procedures, batch records, and other key documents. Your role will also include...
-
Technical Writer
2 months ago
Frederick, United States GForce Life Sciences Full timeJob Title: Technical WriterOnsite in Frederick, MDDuration: 12+ months Job Description: We’re looking for a Technical Writer to help create and update documentation for our biologics manufacturing processes. You’ll be involved in writing and revising standard operating procedures, batch records, and other key documents. Your role will also include...
-
Technical Writer
4 weeks ago
Frederick, Maryland, United States US Tech Solutions Full timeJob Summary:US Tech Solutions is seeking a skilled Technical Writer to support the development of standard operating procedures and technical documentation for our manufacturing processes. The ideal candidate will have experience in biotechnology/pharmaceutical manufacturing and excellent written and verbal communication skills.Responsibilities:Develop and...
-
Technical Writer
2 weeks ago
Frederick, Maryland, United States US Tech Solutions Full timeJob SummaryWe are seeking a skilled Technical Writer to support our GMP upstream and downstream manufacturing process. The ideal candidate will have experience in biotechnology/pharmaceutical manufacturing and excellent written and verbal communication skills.ResponsibilitiesDevelop and maintain standard operating procedures for manufacturing processes and...
-
Technical Writer
4 weeks ago
Frederick, United States GForce Life Sciences Full timeThe Technical Writer is responsible for supporting the overall GMP upstream and downstream manufacturing process, through the application of broad technical writing experiences, developing standard operating procedures for manufacturing processes as well as routine tasks in the production of bulk biologics therapies. • Generates/revises manufacturing batch...
-
Technical Writer
4 weeks ago
Frederick, United States GForce Life Sciences Full timeThe Technical Writer is responsible for supporting the overall GMP upstream and downstream manufacturing process, through the application of broad technical writing experiences, developing standard operating procedures for manufacturing processes as well as routine tasks in the production of bulk biologics therapies. • Generates/revises manufacturing batch...
-
Technical Writer
4 weeks ago
Frederick, United States US Tech Solutions Full timeDuration: 12 Months (Possibility of extension)Job Summary:The Technical Writer is responsible for supporting the overall GMP upstream and downstream manufacturing process, through the application of broad technical writing experiences, developing standard operating procedures for manufacturing processes as well as routine tasks in the production of bulk...
-
Technical Writer
4 weeks ago
Frederick, United States US Tech Solutions Full timeDuration: 12 Months (Possibility of extension)Job Summary:The Technical Writer is responsible for supporting the overall GMP upstream and downstream manufacturing process, through the application of broad technical writing experiences, developing standard operating procedures for manufacturing processes as well as routine tasks in the production of bulk...
-
Technical Writer
3 days ago
Frederick, Maryland, United States Chimera Enterprises International Full timeJob Title: Technical WriterJob Summary:Chimera Enterprises International is seeking a skilled Technical Writer to support the Joint Program Executive Office for Chemical, Biological, Radiological and Nuclear Defense (JPEO-CBRND) JPEO-CBRND Medical Office. The JPEO-CBRND manages our nation's investments in chemical, biological, radiological, and nuclear...
-
Biotechnology Documentation Specialist
4 weeks ago
Frederick, Maryland, United States GForce Life Sciences Full timeJob Title: Technical WriterJoin GForce Life Sciences as a Technical Writer to create and update documentation for our biologics manufacturing processes.Duration: 12+ monthsLocation: Onsite in Frederick, MDJob Description:We're seeking a skilled Technical Writer to develop and maintain accurate and clear documentation for our manufacturing processes. As a key...
-
Biotechnology Documentation Specialist
4 weeks ago
Frederick, Maryland, United States GForce Life Sciences Full timeJob Title: Technical WriterJoin GForce Life Sciences as a Technical Writer and contribute to the creation and update of documentation for our biologics manufacturing processes.Key Responsibilities:Develop and maintain accurate and clear documentation for manufacturing batch records and standard operating procedures.Support the development of documentation...
-
Manufacturing Process Specialist
1 week ago
Frederick, Colorado, United States Agilent Technologies Full timeKey Responsibilities:As a Manufacturing Engineer at Agilent Technologies, you will be responsible for performing a wide range of technical duties to support manufacturing operations. This includes the transfer and scale-up of new processes from Chemical Development, as well as the development and implementation of new manufacturing technologies.Key Skills:...
-
GMP Manufacturing Specialist
4 weeks ago
Frederick, Maryland, United States Intelliswift Software Full timeCell Therapy Specialist Job DescriptionJob Summary:The Cell Therapy Specialist will be responsible for performing and/or verifying all tasks associated with the manufacture of commercial product following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations.Key Responsibilities:Successfully troubleshoots processing...
-
GMP Manufacturing Specialist
4 weeks ago
Frederick, Maryland, United States Intelliswift Software Full timeJob Title: Cell Therapy SpecialistLocation: Frederick, MD Duration: 12 MonthsJob DescriptionThe Cell Therapy Specialist will perform and/or verify all tasks associated with the manufacture of commercial product following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations as part of a team to execute GMP runs in...
-
GMP manufacturing Associate
4 weeks ago
Frederick, United States Intelliswift Software Full timeTitle: Cell Therapy SpecialistLocation: Frederick, MD Duration: 12 MonthsJob DescriptionThe Cell Therapy Specialist will perform and/or verify all tasks associated with the manufacture of commercial product following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations as well as works as part of a team to execute...
-
GMP manufacturing Associate
1 month ago
Frederick, United States Intelliswift Software Full timeTitle: Cell Therapy SpecialistLocation: Frederick, MD Duration: 12 MonthsJob DescriptionThe Cell Therapy Specialist will perform and/or verify all tasks associated with the manufacture of commercial product following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations as well as works as part of a team to execute...
-
GMP manufacturing Associate
1 month ago
Frederick, United States Intelliswift Software Full timeTitle: Cell Therapy SpecialistLocation: Frederick, MD Duration: 12 MonthsJob DescriptionThe Cell Therapy Specialist will perform and/or verify all tasks associated with the manufacture of commercial product following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations as well as works as part of a team to execute...
Manufacturing Technical Writer
2 months ago
Immediate need for a talented Manufacturing Technical Writer. This is a 12+ Months Contract opportunity with long-term potential and is located in Frederick MD(Onsite). Please review the job description below and contact me ASAP if you are interested.
Job ID:24-38604
Pay Range: $45 - $50/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).
Key Responsibilities:
- Generates/revises manufacturing batch records, both in the electronic batch record system (PAS-X) and the document management system
- Generates/revises standard operating procedures and other related documents in clear and easy to understand language.
- May assist with management of change controls in the Quality Management System.
- Technical Writing Support of Upstream, Downstream and Central Services.
- Manage updates and revisions to technical process documentation.
- Interfaces across multiple departments with subject matter experts for review and approval of documentation and changes.
- Self-manages time to complete work based on critical timelines.
Key Requirements and Technology Experience:
- Skills-Cell Culture, Manufactuing, Batch Record.
- Experience in Biotechnology/Pharmaceutical Manufacturing: This is a Manufacturing tech writer; they need to have previous experience in Manufacturing of Pharmaceuticals (Biotech is preferred)
- Excellent Written and Verbal Communication Skills: Clear and effective communication including writing Batch records (paper or electronic) and SOPs.
- Strong Attention to Detail: Given the critical nature of the documents and processes involved, attention to detail is crucial to ensure accuracy and compliance.
- Please make sure candidates have Manufacturing experience either working as Manufacturing Technicians or Manufacturing Associates with direct hands-on experience in manufacturing.
- Previous experience in Biotechnology/Pharmaceutical Manufacturing.
- Excellent written and verbal communication skills.
- Proficiency in MS Office, specifically MS Word and Visio.
- Strong attention to detail.
- Able to write in explanatory and procedural styles for multiple audiences.
- Skilled at prioritization and multi-tasking.
- Proven experience working in a technical writing position preferred.
- Experience with PAS-X/electronic batch records and change management preferred.
- BA preferred.
- Science degree (chemistry, biology, engineering, pharmacy) or experience in Life.
- Sciences technical writing preferred.
Our client is a leading Pharmaceutical Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.