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Document Control Two Jobs in New York (NOW HIRING)

CEDENT

Technical Writer

Springfield, NJ · On-site

Document Management: Assist in the management of controlled documents in document control systems ... Experience: * Minimum of 2 years of experience in technical writing within a GMP-regulated ...

SI Engineering, P.C.

Office Engineer

New York, NY · On-site

$93K - $104K/yr

The successful candidate will manage document control, submittal tracking, as-built drawings, RFI ... A choice of two comprehensive health insurance plans * Dental and Vision Insurance * Term Life ...

SI Engineering PC

Office Engineer

New York, NY · On-site

$93K - $104K/yr

The successful candidate will manage document control, submittal tracking, as-built drawings, RFI ... A choice of two comprehensive health insurance plans * Dental and Vision Insurance * Term Life ...

Getinge

QC Inspector II

Wayne, NJ · On-site

$27 - $30/hr

Document test and inspection results following good documentation practices. * Aid in the return of ... Minimum Requirements * 2 years technical school or equivalent experience. * 3 years minimum ...

Getinge

QC Inspector II

Wayne, NJ · On-site

$27 - $30/hr

Document test and inspection results following good documentation practices. * Aid in the return of ... Minimum Requirements * 2 years technical school or equivalent experience. * 3 years minimum ...

Getinge

QC Inspector II

Wayne, NJ · On-site

$27 - $30/hr

Document test and inspection results following good documentation practices. * Aid in the return of ... Minimum Requirements * 2 years technical school or equivalent experience. * 3 years minimum ...

Formosa Plastics

Auditor II

Livingston, NJ · On-site

$75K - $116K/yr

With annual revenues of more than $5 billion, we employ over 2,800 people who operate 20 production ... the document control process and maintains the Document Center webpage, ensuring proper version ...

Marotta Controls, Inc.

Document Specialist

Montville, NJ · On-site

$33 - $36/hr

Dedicated to innovation, quality and excellence, we deliver cutting edge control systems for the ... Minimum Qualifications * 0-2 years' experience with documentation/inspection in a manufacturing or ...

Marotta Controls, Inc.

Document Specialist

Montville, NJ · On-site

$33 - $36/hr

Dedicated to innovation, quality and excellence, we deliver cutting edge control systems for the ... Minimum Qualifications * 0-2 years' experience with documentation/inspection in a manufacturing or ...

ATD Technology LLC

Financial Analyst

New York, NY · On-site

$70 - $72/hr

... documentation, form design and control, two of which shall have been in data processing and management information systems; * and, General knowledge of computer and communication capabilities ...

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All JobsDocument Control Two JobsDocument Control Two Jobs in New York

Document Control Two information

Is document control a good career path?

Document Control Two is a role that involves managing and organizing company records, ensuring compliance with industry standards, and using document management software. It can be a stable career with opportunities for advancement in industries such as manufacturing, construction, and engineering. Developing skills in attention to detail, organization, and familiarity with quality management systems can enhance career prospects.
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Technical Writer

CEDENT

Springfield, NJ • On-site

Full-time

Re-posted 17 days ago

Job description

Summary: Reporting to the appropriate department based on area of expertise (Quality Assurance, Quality Control, or Manufacturing). We are seeking a detail-oriented and highly skilled GMP Pharmaceutical Technical Writer to join our team. The ideal candidate will be responsible for creating, revising, and maintaining various controlled documentation that complies with Good Manufacturing Practices (GMP) regulations and industry standards. This role will work closely with internal and client cross-functional teams, including quality assurance, regulatory, production, and project management, to ensure timely delivery, accuracy, and clarity of all technical documents essential for the manufacturing and regulatory processes in a pharmaceutical industry.
Responsibilities:
  • Technical Documentation: Author, edit, and maintain a wide range of documents, including Standard Operating Procedures (SOPs), batch records, validation protocols, technical reports, change control documents, and regulatory submissions in accordance with GMP guidelines.
  • Compliance: Ensure all written materials meet regulatory and GMP requirements, and align with the company’s quality standards, procedures, and policies.
  • Collaboration: Work closely with both Client stakeholders and client stakeholders to establish alignment on deliverables and ensure project timelines are maintained.
  • Document Management: Assist in the management of controlled documents in document control systems (e.g., electronic document management systems), ensuring traceability, version control, and appropriate distribution of approved documents.
  • Process Improvement: Participate in process improvement initiatives related to document control, writing standards, and compliance, ensuring continuous enhancement of documentation practices.
  • Audits & Inspections: Support internal and external audits by preparing relevant documentation and ensuring that all technical writing adheres to current regulatory standards.
  • Change Control: Document and track changes in manufacturing processes, equipment, and methodologies, ensuring updates to procedures and records are properly reflected.
Essential Education and Qualifications:
  • Education: Bachelor's degree in Life Sciences, Chemistry, Pharmaceutical Sciences, Engineering, or a related field. Advanced degree or certification in technical writing is a plus.
  • Experience:
  • Minimum of 2 years of experience in technical writing within a GMP-regulated environment in the pharmaceutical, biotech, or related industry.
  • Experience writing technical documentation, including SOPs, validation protocols, and reports.
  • Knowledge:
  • Solid understanding of GMP regulations (FDA, EMA, ISO, ICH, etc.) and regulatory requirements for pharmaceutical manufacturing.
  • Proficiency with document management systems and Microsoft Office Suite (Word, Excel, PowerPoint).
  • Skills:
  • Exceptional written and verbal communication skills, with a strong ability to translate complex technical concepts into clear, concise documentation.
  • Detail-oriented with strong organizational and project management skills.
  • Ability to work independently, manage multiple projects simultaneously, and meet deadlines in a fast-paced environment.
  • Strong analytical and problem-solving skills, with the ability to work cross-functionally across departments.
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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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