Copy writer Jobs in College Station, TX

Job details Spherion Staffing is partnering with a major biotech client to find a highly skilled Technical Writer. Our client is a leading organization in the biotech industry, known for its innovative approach and commitment to excellence. We are looking for a detail-oriented and experienced Technical Writer to join their team.

Responsibilities : ... Create, revise, and maintain technical documents, including user manuals, SOPs, guidelines, and reports.

Conduct thorough research to identify deviations and inconsistencies in the workflow process.

Collaborate with cross-functional teams to gather technical information and ensure accuracy in documentation.

Review and analyze technical data, specifications, and project requirements to produce clear and concise documents.

Ensure all documents comply with company standards, regulatory requirements, and industry best practices.

Proofread and edit content for grammar, format, and clarity, ensuring the highest level of detail and precision.

Manage multiple writing projects simultaneously and meet deadlines consistently.

Utilize various tools and software to create and manage documentation.

Working hours : 8 : 00 AM - 5 : 00 PM (Various Shifts Available)

Skills :

3+ years of experience.

Education : Bachelors

Experience : 1-4 years

Qualifications : CGMP experience

Proven experience in technical writing, preferably in the biotech or pharmaceutical industry.

Exceptional attention to detail and a meticulous approach to documentation.

Strong ability to conduct detailed research and analyze workflow processes to detect deviations.

Excellent written and verbal communication skills.

Proficiency in technical writing tools and software.

Ability to understand and convey complex technical information clearly and accurately.

Strong organizational and time-management skills.

Bachelor's degree in Technical Writing, Life Sciences, Engineering, or a related field is preferred.

Apply today! We look forward to reviewing your application!Show lessShow more Spherion Staffing is partnering with a major biotech client to find a highly skilled Technical Writer. Our client is a leading organization in the biotech industry, known for its innovative approach and commitment to excellence. We are looking for a detail-oriented and experienced Technical Writer to join their team.

Responsibilities :

Create, revise, and maintain technical documents, including user manuals, SOPs, guidelines, and reports.

Conduct thorough research to identify deviations and inconsistencies in the workflow process.

Collaborate with cross-functional teams to gather technical information and ensure accuracy in documentation.

Review and analyze technical data, specifications, and project requirements to produce clear and concise documents.

Ensure all documents comply with company standards, regulatory requirements, and industry best practices.

Proofread and edit content for grammar, format, and clarity, ensuring the highest level of detail and precision.

Manage multiple writing projects simultaneously and meet deadlines consistently.

Utilize various tools and software to create and manage documentation.

• Working hours : 8 : 00 AM - 5 : 00 PM (Various Shifts Available)

Skills :

3+ years of experience.

Education : Bachelors

Experience : 1-4 years

Qualifications : CGMP experience

Proven experience in technical writing, preferably in the biotech or pharmaceutical industry.

Exceptional attention to detail and a meticulous approach to documentation.

Strong ability to conduct detailed research and analyze workflow processes to detect deviations.

Excellent written and verbal communication skills.

Proficiency in technical writing tools and software.

Ability to understand and convey complex technical information clearly and accurately.

Strong organizational and time-management skills.

Bachelor's degree in Technical Writing, Life Sciences, Engineering, or a related field is preferred.

Apply today! We look forward to reviewing your application!Show lessShow more

key responsibilities

Create, revise, and maintain technical documents, including user manuals, SOPs, guidelines, and reports.Conduct thorough research to identify deviations and inconsistencies in the workflow process.Collaborate with cross-functional teams to gather technical information and ensure accuracy in documentation.Review and analyze technical data, specifications, and project requirements to produce clear and concise documents.Ensure all documents comply with company standards, regulatory requirements, and industry best practices.Proofread and edit content for grammar, format, and clarity, ensuring the highest level of detail and precision.Manage multiple writing projects simultaneously and meet deadlines consistently.Utilize various tools and software to create and manage documentation.

experience

1-4 years

skills

3+ years of experience.

qualifications

CGMP experienceProven experience in technical writing, preferably in the biotech or pharmaceutical industry.Exceptional attention to detail and a meticulous approach to documentation.Strong ability to conduct detailed research and analyze workflow processes to detect deviations.Excellent written and verbal communication skills.Proficiency in technical writing tools and software.Ability to understand and convey complex technical information clearly and accurately.Strong organizational and time-management skills.Bachelor's degree in Technical Writing, Life Sciences, Engineering, or a related field is preferred.

education

Bachelors