Job Description
ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science companies researching, developing, and manufacturing innovative products to serve patients and respond to public health challenges around the world. ELIQUENT is committed to serving clients’ needs with extensive expertise, unwavering integrity, and strategic insight in a manner that supports availability of safe, effective, and high-quality drugs, biologics, and medical devices. For more information, please visit our website at eliquent.com.
The ETHOS Program is a foundational training, mentorship, and development program designed to prepare early‑career professionals to navigate complex Life Science projects and contribute to ELIQUENT’s mission and client success.
An ETHOS Consultants' primary responsibility is to provide clients with professional services under supervision.
Responsibilities:
Technical Writing
• Write technical documentation for clients under supervision including but not limited to:
• Writing procedures, investigations, protocols, reports, change controls, CAPAs, etc. to support the Maintenance, Engineering, Validation, Quality, and Regulatory departments. Documents are reviewed by mentors or senior consultants.
• Generating validation documents for qualification of facilities, utilities, equipment or instruments and processes including cleaning, sterilization, shipping, and manufacturing including protocols and reports. Documents are reviewed by mentors or senior consultants.
• Writing and revising technical documents to support qualification activities including SOPs, validation/verification master plans, guidelines and execution plans, automation test plans, engineering design reviews, commissioning, user requirement specifications (URS), functional requirement specifications (FRS), detailed design specifications, factory acceptance test documents (FAT), site acceptance test (SAT) and/or commissioning test procedures.
Service Delivery
• Performs on site or support work for a client under supervision, including but not limited to:
• Qualification and Validation protocol execution
• Thermal mapping of temperature-controlled chambers, warehouses, and sterilization processes
• Investigations and deviations
• Risk analysis, and/or failure mode and affect analysis
• Data integrity assessments and review of client data
• Executes protocols and helps resolve deviations/discrepancies, analyze study data and write summary reports, under supervision of senior consultants.
Problem Solving
• Provides solutions to routine technical problems with limited scope under supervision of senior consultants.
• Supports the resolution of regulatory observations or manufacturing site issues.
Time Management
• Responsible for tracking time to budget and notifying supervisors of any issues on deliverables.
• Carries out duties in compliance with all local, state, and federal regulations and guidelines including the FDA, EPA, and OSHA.
• Complies with all internal and client site policies and procedures.
• Successfully completes job training requirements.
• Individuals must represent Eliquent at client sites and interact confidently with clients, contractors, management and peers.
Requirements, Education, and Qualifications:
• Maintains technical knowledge by attending educational workshops and/or reviewing publications
• Other duties as assigned by Sr. Management
Quality:
• Adhere to all Standard Operating Procedures (SOPs) and Good Manufacturing Practice (GMP).
Training & Development:
• Ensure training has been received before undertaking specific duties and that all training is documented in training records.
Health & Safety:
• Understand the company’s Health & Safety Policy and follow all associated procedures.Report all accidents or awareness of any unsafe conditions in the workplace to supervisor or management.
Human Resource Management:
• Conform to the company’s policies contained in the Employee Handbook
• Familiarity with aspects of validation
• Ability to interpret and carry out instructions furnished in written, oral, diagram, mathematical, or schedule form
• Ability to define problems, collect data, establish facts and draw valid conclusions
• Proficient in Microsoft Word, Excel, and PowerPoint
• Basic understanding of FDA and cGMP regulations and documentation practices
• Familiarity with pharmaceutical manufacturing or bioprocessing equipment
• Familiarity with laboratory instrumentation
Preferred experience:
• Work or internship in a regulated industry such as pharmaceuticals, biotechnology, or medical device
Required Education:
• Bachelor's degree in engineering (Chemical, Biomedical, Mechanical) preferred, Bachelor’s in biology or chemistry may be considered with additional experience.
Additional Qualifications:
• Customer service/client relations
• Communication proficiency
• Attention to detail
• Can work productively independently with minor supervision
• Self-motivated, flexible, dependable and available
• Excellent organizational and time management skills
What We Offer:
• Competitive Compensation: Attractive salary and comprehensive benefits package for full-time and part-time employees, including health, dental, vision, and life insurance, a 401(k) plan with employer match, a generous paid time off policy, and additional perks. Compensation is commensurate with professional experience.
• Career Development: Opportunities for professional growth and advancement within a supportive and innovative environment.
• Work-Life Balance: Flexible work arrangements and a commitment to maintaining a healthy work-life balance.
Eliquent Life Sciences is proud to be an Equal Opportunity Employer, committed to employee diversity.
Salary: 75k-80k
The ETHOS Program is a foundational training, mentorship, and development program designed to prepare early‑career professionals to navigate complex Life Science projects and contribute to ELIQUENT’s mission and client success.
An ETHOS Consultants' primary responsibility is to provide clients with professional services under supervision.
Responsibilities:
Technical Writing
• Write technical documentation for clients under supervision including but not limited to:
• Writing procedures, investigations, protocols, reports, change controls, CAPAs, etc. to support the Maintenance, Engineering, Validation, Quality, and Regulatory departments. Documents are reviewed by mentors or senior consultants.
• Generating validation documents for qualification of facilities, utilities, equipment or instruments and processes including cleaning, sterilization, shipping, and manufacturing including protocols and reports. Documents are reviewed by mentors or senior consultants.
• Writing and revising technical documents to support qualification activities including SOPs, validation/verification master plans, guidelines and execution plans, automation test plans, engineering design reviews, commissioning, user requirement specifications (URS), functional requirement specifications (FRS), detailed design specifications, factory acceptance test documents (FAT), site acceptance test (SAT) and/or commissioning test procedures.
Service Delivery
• Performs on site or support work for a client under supervision, including but not limited to:
• Qualification and Validation protocol execution
• Thermal mapping of temperature-controlled chambers, warehouses, and sterilization processes
• Investigations and deviations
• Risk analysis, and/or failure mode and affect analysis
• Data integrity assessments and review of client data
• Executes protocols and helps resolve deviations/discrepancies, analyze study data and write summary reports, under supervision of senior consultants.
Problem Solving
• Provides solutions to routine technical problems with limited scope under supervision of senior consultants.
• Supports the resolution of regulatory observations or manufacturing site issues.
Time Management
• Responsible for tracking time to budget and notifying supervisors of any issues on deliverables.
• Carries out duties in compliance with all local, state, and federal regulations and guidelines including the FDA, EPA, and OSHA.
• Complies with all internal and client site policies and procedures.
• Successfully completes job training requirements.
• Individuals must represent Eliquent at client sites and interact confidently with clients, contractors, management and peers.
Requirements, Education, and Qualifications:
• Maintains technical knowledge by attending educational workshops and/or reviewing publications
• Other duties as assigned by Sr. Management
Quality:
• Adhere to all Standard Operating Procedures (SOPs) and Good Manufacturing Practice (GMP).
Training & Development:
• Ensure training has been received before undertaking specific duties and that all training is documented in training records.
Health & Safety:
• Understand the company’s Health & Safety Policy and follow all associated procedures.Report all accidents or awareness of any unsafe conditions in the workplace to supervisor or management.
Human Resource Management:
• Conform to the company’s policies contained in the Employee Handbook
• Familiarity with aspects of validation
• Ability to interpret and carry out instructions furnished in written, oral, diagram, mathematical, or schedule form
• Ability to define problems, collect data, establish facts and draw valid conclusions
• Proficient in Microsoft Word, Excel, and PowerPoint
• Basic understanding of FDA and cGMP regulations and documentation practices
• Familiarity with pharmaceutical manufacturing or bioprocessing equipment
• Familiarity with laboratory instrumentation
Preferred experience:
• Work or internship in a regulated industry such as pharmaceuticals, biotechnology, or medical device
Required Education:
• Bachelor's degree in engineering (Chemical, Biomedical, Mechanical) preferred, Bachelor’s in biology or chemistry may be considered with additional experience.
Additional Qualifications:
• Customer service/client relations
• Communication proficiency
• Attention to detail
• Can work productively independently with minor supervision
• Self-motivated, flexible, dependable and available
• Excellent organizational and time management skills
What We Offer:
• Competitive Compensation: Attractive salary and comprehensive benefits package for full-time and part-time employees, including health, dental, vision, and life insurance, a 401(k) plan with employer match, a generous paid time off policy, and additional perks. Compensation is commensurate with professional experience.
• Career Development: Opportunities for professional growth and advancement within a supportive and innovative environment.
• Work-Life Balance: Flexible work arrangements and a commitment to maintaining a healthy work-life balance.
Eliquent Life Sciences is proud to be an Equal Opportunity Employer, committed to employee diversity.
Salary: 75k-80k
💡 Quick Summary
Seeking a career-building opportunity? The Consultant 1 - Technical Writer position is now open for candidates interested in the Content Writer Jobs sector. This role in Los Angeles offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Content Writer Jobs is a plus.
