Chemistry Job Alert

The pharmaceutical industry regularly offers new opportunities for professionals in analytical development, research, and regulatory documentation. For candidates who have experience in analytical laboratories and documentation work, a new opportunity has been announced by Eris Therapeutics.

The company is currently hiring for the position of ADL Documentation Executive / Senior Officer. This role is suitable for candidates who have qualifications in pharmaceutical sciences or analytical chemistry and experience working in documentation related to analytical laboratories or R&D departments.

In this article, we will explain the complete details about the job role, qualification, required skills, responsibilities, and the application process in simple language so that interested candidates can understand the opportunity clearly.

About the Company

Eris Therapeutics is a pharmaceutical organization involved in developing and manufacturing medicines. Companies working in the pharmaceutical sector require strong analytical and documentation teams to ensure that all processes follow regulatory guidelines.

In pharmaceutical industries, proper documentation is extremely important because every experiment, test result, and development process must be recorded accurately. This documentation helps companies maintain compliance with international quality standards and regulatory authorities.

That is why professionals who have good analytical knowledge and documentation skills are always in demand in this field.

Job Position Details

The company has opened positions for the following role:

Position: ADL Documentation Executive / Senior Officer

This role focuses mainly on documentation activities in the Analytical Development Laboratory (ADL). The person working in this position will be responsible for preparing analytical documents, reviewing reports, and ensuring that all documentation follows regulatory guidelines.

Candidates with analytical laboratory experience and strong technical writing skills can perform well in this position.

Educational Qualification

To apply for this position, candidates should have one of the following educational qualifications:

M.Sc in Analytical Chemistry or Pharmaceutical Sciences

B.Pharm

M.Pharm

Candidates who have studied pharmaceutical sciences, analytical chemistry, or related subjects will be suitable for this role.

During their studies, candidates usually learn about analytical instruments, pharmaceutical testing, and laboratory documentation. This knowledge becomes very useful when working in analytical development laboratories.

Experience Required

The company is looking for professionals who already have some experience in the pharmaceutical industry.

Required Experience: 2 to 6 years

Candidates who have worked in ADL or R&D documentation roles will have an advantage. Experience in preparing analytical reports, reviewing laboratory documents, and maintaining regulatory compliance is very valuable for this position.

Professionals who have worked in pharmaceutical companies, contract research organizations, or analytical laboratories can apply for this role.

Knowledge of Analytical Instruments

For this position, candidates should have knowledge of analytical techniques commonly used in pharmaceutical laboratories.

Some important instruments and techniques include:

High Performance Liquid Chromatography

Gas Chromatography

Dissolution testing

Other analytical laboratory techniques

Understanding these instruments helps candidates interpret laboratory results and prepare proper analytical reports.

Regulatory and Documentation Knowledge

Pharmaceutical companies follow strict regulatory guidelines to maintain product quality and safety. Therefore, candidates should have knowledge of regulatory documentation requirements.

Some important regulatory authorities and guidelines include:

International Council for Harmonisation

U.S. Food and Drug Administration

Understanding these guidelines helps professionals prepare documentation that meets international regulatory standards.

Candidates should also be familiar with regulatory filing documentation, which is used during drug approval and submission processes.

Key Skills Required

To succeed in this role, candidates should possess a combination of technical knowledge and documentation skills.

Technical Writing Skills

Documentation professionals need to prepare clear and accurate reports. Therefore, strong technical writing skills are essential for this position.

The ability to write analytical procedures, protocols, and reports in a clear format is very important.

Data Review and Analytical Reporting

Candidates should also have the ability to review analytical data and prepare reports. This involves checking laboratory results and ensuring that all data is properly recorded and verified.

Accurate data review helps maintain the quality and reliability of pharmaceutical research.

Computer Skills

Candidates should have good knowledge of basic computer tools used in documentation work, including:

Microsoft Word

Microsoft Excel

These tools are commonly used for preparing reports, maintaining data records, and managing documentation systems.

Key Responsibilities

The selected candidates will be responsible for several important tasks related to analytical documentation.

Preparation of Analytical Documents

One of the main responsibilities of this role is preparing documents such as:

Specifications

STPs (Standard Test Procedures)

Analytical protocols

Analytical reports

These documents are important for recording laboratory testing procedures and results.

Coordination with Different Departments

Documentation professionals often work closely with different departments in the pharmaceutical industry.

This includes coordination with:

Quality Assurance (QA)

Quality Control (QC)

Research and Development (R&D)

Working with multiple teams ensures that documentation activities are completed accurately and efficiently.

Ensuring Regulatory Compliance

Another key responsibility is ensuring that all documentation follows regulatory guidelines.

Pharmaceutical companies follow cGMP (Current Good Manufacturing Practices) to maintain product quality and safety. Documentation teams help ensure that laboratory records meet these standards.

Maintaining proper compliance helps companies pass regulatory inspections and audits.

Why This Job Opportunity is Valuable

This job role can be a good opportunity for professionals who want to build a career in pharmaceutical documentation and analytical development.

Some benefits of working in such roles include:

Exposure to pharmaceutical research and analytical laboratories

Experience in regulatory documentation

Opportunity to work with QA, QC, and R&D teams

Career growth in pharmaceutical regulatory and analytical fields

Professionals who gain experience in ADL documentation often grow into senior positions in regulatory affairs, analytical development, or quality systems.

How to Apply

Interested candidates can apply for this position by sending their updated resume to the recruitment email provided by the company.

Email: recruitment@eristherapeutics.com

Candidates should ensure that their resume clearly mentions their:

Educational qualification

Work experience

Knowledge of analytical instruments

Documentation experience

Contact details

A well-prepared resume increases the chances of getting shortlisted for the interview process.

Final Thoughts

The pharmaceutical industry depends heavily on accurate laboratory documentation and regulatory compliance. Professionals who have strong analytical knowledge and documentation skills are highly valuable for pharmaceutical companies.

The ADL Documentation Executive / Senior Officer role at Eris Therapeutics provides a good opportunity for candidates with M.Sc, B.Pharm, or M.Pharm qualifications and 2–6 years of experience in pharmaceutical documentation.

If you have experience working in analytical laboratories and documentation activities, this opportunity could help you advance your career in the pharmaceutical industry.

Interested candidates should review the job requirements carefully and apply with their updated resume.