What Jobs are available for Pharmaceutical in Thailand?

Regulatory Affairs Manager (Regional)

Location: Bang Phli, Samut Prakan

Are you a regulatory affairs professional with expertise in the chemical or pharmaceutical industry, particularly in cleaning and hazardous substances? Join our global team as a Regulatory Affairs Manager - ASEAN and take a leading role in driving compliance, innovation, and collaboration across Southeast Asia.

• Provide regulatory guidance and support for commercial, technical, and product-related activities.
• Manage product registrations, labeling, SDS, and documentation in line with ASEAN regulatory frameworks.
• Build and maintain strong relationships with regulatory authorities, industry bodies, and strategic partners.
• Support supply chain and manufacturing partners with compliance requirements.
• Supervise and develop regulatory staff as assigned.
• Partner with business development and R&D teams on new product initiatives.
• Deliver regular reports and updates to the Global Regulatory Affairs Manager.
• Travel within ASEAN as required.

• Minimum 5 years' experience in Regulatory Affairs, with at least 2 years at Regional supervisor level.
• Strong background in the chemical or pharmaceutical industry, ideally in cleaning products or hazardous substances.
• Proven track record managing regional regulatory affairs across ASEAN.
• Strong knowledge of ASEAN compliance requirements for pesticides, hazardous substances, or related chemical regulations.
• Excellent stakeholder management and problem-solving skills.
• Fluent in English, both written and spoken; additional ASEAN languages are an advantage.
• Ability to work independently and effectively within a global matrix organization.

Our client, a Leading multinational pharmaceutical company, is seeking an experienced Regulatory Affairs Manager to lead and oversee all regulatory activities in Thailand. This role is critical in ensuring compliance, driving successful product registrations, and maintaining strong relationships with the Thai FDA.

• Manage all activities related to product registration for pharmaceutical products, OTC, medical devices, cosmetics, food, chemicals, and biologics.
• Review, evaluate, and coordinate product documentation, ensuring all requirements for product registration are met.
• Ensure all submissions and approvals comply with local laws, regulations, and guidelines.
• Communicate approvals or regulatory changes effectively across relevant internal and external stakeholders.
• Build and maintain strong relationships with government agencies, proactively influencing and responding to regulatory developments.
• Identify regulatory and quality risks, proposing preventive and corrective strategies for product registrations.
• Stay updated on evolving regulations, laws, and competitive landscapes to provide timely regulatory intelligence.
• Manage and coordinate Pharmacovigilance activities in compliance with Thai FDA requirements.
• Ensure proper documentation of registered products.
• Lead, develop, and coach the Regulatory Affairs team to achieve goals and deliver key objectives on time.

• Bachelor's or Master's degree in Pharmacy.
• Licensed Pharmacist (mandatory).
• Minimum 5 years of experience in Regulatory Affairs within the pharmaceutical or healthcare industry (PHC/CHC).
• Proven experience with product registration for pharmaceuticals, biologics, medical devices, cosmetics, foods, and related categories.
• Strong working relationship with the Thai FDA and demonstrated success in regulatory negotiations.
• Excellent networking, communication, and result-oriented skills.
• Strong analytical and problem-solving skills with the ability to resolve regulatory challenges.
• Proficient in MS Office and fluent in English (spoken, written, and read).

The ideal candidate will have:

• In-depth knowledge of regulatory compliance and local requirements for product registration.
• Strong leadership, team management, and coaching skills.
• Ability to analyze complex regulatory issues and deliver practical solutions.
• Proactive mindset with strong influence and stakeholder management abilities.

Responsibilities:

• Responsible for medical product registration, renewals, post-approval changes, and advertisement approvals with Thai FDA
• Prepare and compile registration dossiers and related documents in line with Thai FDA requirements
• Coordinate with internal teams on submission status and regulatory updates
• Ensure all necessary documents are prepared on time to meet submission deadlines
• Submit and follow up with Thai FDA to obtain timely approvals
• Maintain compliance with ISO 13485 and relevant standards/regulations

Qualifications:

• Bachelor's Degree in Science, Medical or related fields.
• 3 years of experience in Medical Device products registration process or related field.
• Knowledge of registration process and/ or DCC for any applicable QMS (ISO13485).
• Have good experience in working with FDA in preparation of documents for the product registration until product marketing approval.

MAIN PURPOSE OF ROLE

Summarize the main purpose of the role.

Individual contributor that works under limited supervision and applies subject matter knowledge to support the promotion and/or selling of the organization's products across multiple or non-specified channels in a designated territory by contacting specialists, physicians, pharmacies and/or distributors.

MAIN RESPONSIBILITIES

• Arranges appointments with doctors, pharmacists and hospital medical teams, which may include pre-arranged appointments or 'cold' calling.
• Organises conferences for doctors and other medical staff.
• Builds and maintains positive working relationships with medical staff and supporting administrative staff.
• Keeps detailed records of all contacts.
• Regularly attends company meetings, technical data presentations and briefings.
• Keeps up to date with the latest clinical data supplied by the company, and interpreting, presenting and discussing this data with health professionals during presentations.

Education Level

High School Diploma / GED

Experience

Minimum 2 years

We are creators, culture-shakers, and makers of the internet's favorite stuff. We live and breathe social, move fast, and thrive on pushing boundaries. Our team is obsessed with what we do, and now we're looking for someone who's just as fired up about the influencer world as we are.

Are you plugged into Thailand's influencer scene, fluent in both Thai and English, and ready to jump into a fast-paced project? This short-term but high-impact opportunity is your chance to collaborate with a global team while owning influencer strategy and execution in Thailand.

Here's where you come in:

• Research, source, and recommend influencers/KOLs that align with project briefs and campaign goals.
• Manage relationships with influencers, from negotiation and contracting to ensuring smooth content delivery.
• Develop influencer content principles and briefing guides for campaigns, ensuring assets are authentic, engaging, and platform-ready.
• Collaborate on creative direction for influencer video and photo production, including shooting guides and platform-specific content recommendations.
• Support cross-market influencer activations in APAC, with potential for global reapplication of best practices.
• Ensure brand equity is at the heart of influencer activations while keeping content engaging and true to platform culture.

What you'll bring:

• 3+ years' experience in influencer/KOL marketing in Thailand.
• Deep knowledge of the local influencer landscape, from micro creators to celebrities.
• Proven ability to write clear, compelling briefs and communicate effectively with talent.
• Experience working on large brand campaigns and activations.
• Familiarity with influencer rights and contracting (a strong plus).
• Established relationships with influencers and talent in Thailand (bonus if you're also a creator yourself).
• Ability to think strategically, balancing local insight with regional/global context.
• Fluency in Thai and English.

The Gig

This is a
full-time contract role based in Bangkok
, available
ASAP until November 7
. If you're passionate about influencer marketing, thrive in high-energy environments, and love making things happen, we'd love to hear from you.

About Us

Kobkiat Global is a pioneering biotechnology company specializing in the sustainable production and utilization of Black Soldier Fly (BSF) larvae. Our innovative approach addresses critical environmental challenges by transforming organic waste into high-quality protein and fertilizer, contributing to a circular economy and sustainable agricultural practices.

We are also leading company in the collection and recycling of used cooking oil. We are dedicated to providing sustainable solutions for waste oil management, transforming waste into valuable resources such as biodiesel, animal feed, and industrial products. Our commitment to environmental stewardship helps reduce pollution and promotes a circular economy.

Job Overview

The GMP+ Compliance Implementer will be responsible for developing, implementing, and maintaining the GMP+ quality assurance program within the organization. This role involves collaborating with various departments to ensure compliance with GMP+ standards, conducting audits, and providing training to staff on GMP+ requirements. The ideal candidate will have a strong background in quality assurance, regulatory compliance, and experience with GMP+ standards. You also will be responsible for our ISCC (International Sustainability and Carbon Certification) Implementation on and developing, implementing, and maintaining the ISCC certification program within the organization.

Key Responsibilities

• Develop and implement GMP+ compliance programs, policies, and procedures.
• Conduct regular internal audits to ensure compliance with GMP+ standards and identify areas for improvement.
• Collaborate with various departments to ensure GMP+ requirements are integrated into all processes and operations.
• Provide training and support to staff on GMP+ standards and compliance requirements.
• Prepare and maintain documentation related to GMP+ compliance, including audit reports, corrective action plans, and compliance records.
• Monitor and stay updated on changes in GMP+ regulations and standards, ensuring the company remains compliant.
• Work with external auditors and regulatory bodies during inspections and audits.
• Investigate and resolve compliance issues, implementing corrective and preventive actions as needed.
• Develop and maintain a culture of quality and continuous improvement within the organization.
• Conduct internal audits to ensure compliance with ISCC standards and identify areas for improvement.
• Collaborate with various departments to integrate ISCC requirements into all processes and operations.
• Provide training and support to staff on ISCC standards and compliance requirements.
• Prepare and maintain documentation related to ISCC compliance, including audit reports, corrective action plans, and compliance records.

Qualifications

• Bachelor's degree in a related field (e.g., Quality Assurance, Regulatory Affairs, Food Science, or a similar discipline).
• 2 to 5 years of experience in quality assurance or regulatory compliance and audit preparation work, preferably within the food or feed industry.
• In-depth knowledge of GMP+ standards and requirements.
• Experience in conducting internal audits and working with external auditors.
• Strong analytical, problem-solving, and organizational skills.
• Excellent communication and interpersonal skills, with the ability to train and motivate staff.
• Detail-oriented with a commitment to maintaining high standards of quality and safety.
• Ability to work independently and as part of a team in a fast-paced environment.
• Certification in GMP+ or related quality assurance programs is a plus.
• In-depth knowledge of ISCC standards and requirements is a pre but not necessary.
• Good English communication skills to collaborate with key stakeholders.

Benefits:

• Competitive salary and benefits package.
• Opportunities for professional development and growth.
• Collaborative and supportive work environment.
• Commitment to work-life balance.

Job Description

Responsible on Griffith Management System (Document control), Religious compliance and supportive on Food Safety and Quality system to meet law/regulatory, company requirements and customer expectation.

Task and Responsibilities

• To oversee and manage the procurement, analysis and optimization of raw materials) and work closely with internal stakeholders, supplier and cross function teams to ensure the consistent supply of high-quality material while also optimizing costs and ensuring the highest standard of quality and compliance and control QC team of raw material, Batching and loading.
• To create and implement a system for identifying, assessing, monitoring and reviewing raw material risk assessment, all can follow Procedure, and questionnaire related with raw material such as PCFM process.
• Supporting LEAN activities and standards such as ISO14001, ISO 45001 , GHP and BRC required as standard and customer requirement to integrate continuous improvement.
• Provide and maintain comprehensive documents on raw material to comply with our requirements on existing and new.
• Advise the QA team on matters related to daily work problems and solve problems that arise.
• Other job assigns to support business.

Qualifications

• Bachelor's degree or Higher in Food Technology, Food Science, related field.
• 3 years' experience in food industry in quality or operations function.

Key Competencies

• Result Orientation
• Continuous Learning
• Customer Oriented
• Adaptability
• Strong leaderships, communication, analytical, and negotiation skill
• High executive maturity and adaptability
• Good command of English and computer literate

Location:  Griffith Foods, Warehouse at Bang Bo Plant

Responsibilities:

•    Maintenance of the Affiliate PV System Country Chapter and additional local PV procedures, forms, and templates

•    PV business continuity planning and notification of any business interruptions that pose a threat locally or globally to pharmacovigilance processes or endanger regulatory compliance

•    Receipt, recording, and reconciliation of safety information

•    Safety surveillance including literature and health authority website screening and preparation of local periodic safety reports and Risk Management Plans

•    Regulatory submission of safety information

•    Basic PV training of local EPD staff

•    PV record retention and archiving

•    Implementation of out-of-office coverage for receiving and recording safety-relevant information

•    Maintenance of local PV product list

•    Ensure PV matters in local interventional studies and local non-interventional organized data collection schemes

•    Negotiation and implementation of local commercial pharmacovigilance agreements and local pharmacovigilance service agreements

•    Due Diligence for product acquisition or in-licensing negotiated by an Affiliate organization

•    Provision of local PV Compliance metrics and management of non-compliances

•    Coordination/management of PV audits and inspections at the Affiliate level

•    Ensure vigilance compliant to local legislation for EPD products beyond medicinal products such as medical devices and food supplements

•    Support in preparation of Health Hazard Assessment/Medical Expert Statements

•    Perform PV quality checks requiring four-eye review

Qualifications:

•    Graduate with a Life Sciences or Pharmacy degree or equivalent qualification

• years of experience in PV

•    PV experience in pharmaceutical company is preferred

•    Understanding of local PV regulation

•    Ability to give attention to the detail

•    Computer literacy (Windows, MS Office)

•    Good English language skills

•    Good communication skills with internal and external stakeholders