46 Pharmaceutical jobs in Thailand

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.

About the Role

We are seeking a
Regulatory Affairs Specialist
with strong expertise in
Thailand NDA/BLA submissions
to join our growing team in Bangkok. This role is critical in driving
end-to-end product registration
for novel drugs and biologics, while serving as a key liaison between
local regulatory bodies (TFDA)
and
China HQ
.

Key Responsibilities

Product Registration (End-to-End)

• Lead full-cycle registration for
  new drugs and biologics
• Collaborate with China HQ to prepare
  TFDA-compliant dossiers
• Manage and maintain
  CTD documents
  throughout the product lifecycle
• Track registration status and ensure
  timely submissions
• Liaise with
  TFDA
  to expedite approvals
• Support feasibility assessments for new product launches

Regulatory Strategy

• Monitor changes in
  Thai regulatory landscape
  , especially for
  innovative drug pathways
• Research local guidelines to support HQ strategy
• Provide
  regulatory intelligence
  to internal stakeholders

Cross-Functional Collaboration

• Coordinate with internal teams (BD, Operations) and external partners
• Align regulatory processes with
  regional marketing
• Escalate critical updates (e.g., TFDA queries, approval milestones) to HQ
• Participate in
  company-wide strategic projects

Qualifications

• Bachelor's degree or higher in
  Pharmacy, Biology
  , or related field
• Hold Pharmacist License in Thailand

• Experience:

• 1-2 years in
  R&D
  , with hands-on experience in
  CMC documentation (Modules 2-3)

• Experience with
  GMP
  in both
  PICS
  and
  non-PICS
  environments
• 3+ years in
  NDA/BLA submissions
  for chemical and biological products
• Successfully led
  ≥2 novel drug registrations
  from submission to approval
• Familiarity with
  CMC, R&D, or clinical development
• Skilled in:
  • Independent
    regulatory dossier authoring
  • CTD gap analysis
  • eCTD
    preparation and submission
• Strong understanding of Thailand Drug Act and related regulations
• Fluent in English (daily communication with China HQ)
• Able to work effectively across cultures
• Willing to travel frequently to China

Responsibilities:

• Develop and implement quality assurance policies and procedures in accordance with regulatory standards, including PIC/s and ISO 9001 requirements.
• Establish and maintain a comprehensive quality management system (QMS) to ensure compliance with all applicable regulations and guidelines.
• Conduct thorough investigations into deviations and non-conformities, identifying root causes and implementing corrective and preventive actions (CAPA) to address underlying issues.
• Collaborate closely with cross-functional teams to implement preventive measures and improve processes to minimize the occurrence of deviations and non-conformities.
• Oversee validation activities for manufacturing processes, equipment, facilities, and computer systems, ensuring compliance with regulatory requirements and industry best practices.
• Ensure the company is capable of undergoing audits by both customers and regulatory authorities, both domestically and internationally.
• Manage document control processes, including the development, review, approval, distribution, and maintenance of quality-related documents and records.
• Provide comprehensive training and ongoing guidance to personnel involved in manufacturing processes, ensuring their full awareness and understanding of quality assurance principles and practices.
• Collaborate with cross-functional teams to resolve quality-related issues and implement preventive measures to mitigate risks.
• Monitor key performance indicators (KPIs) to track and measure quality performance, implementing strategies to enhance product quality and safety.
• Serve as a subject matter expert on quality assurance matters, providing guidance and support to internal stakeholders as needed.

Qualification:

• Bachelor's degree in pharmaceutical science
• Minimum of 8 years of progressive experience in quality assurance roles within the pharmaceutical or related industry, with a solid understanding of regulatory standards and requirements, including PIC/s and ISO 9001.
• In-depth knowledge of regulatory requirements governing pharmaceutical manufacturing and quality assurance, including FDA, EMA, PMDA, PIC/s, and ISO 9001 guidelines.
• Excellent problem-solving skills with a proactive approach to identifying and resolving quality-related issues, as well as implementing preventive measures to mitigate risks.
• Experience in validation activities, including process validation, equipment qualification, and computer system validation.
• Proficiency in document control processes and systems, with experience managing quality-related documents and records.
• Strong leadership and managerial skills, with the ability to effectively lead and develop a high-performing team.
• Excellent communication and interpersonal skills, with the ability to collaborate effectively with internal and external stakeholders at all levels.
• Demonstrated ability to drive process improvements and implement best practices to enhance quality and compliance.

Employee Benefits

• Comprehensive Medical Coverage
• Annual Health Check-ups
• Provident Fund
• Uniform Allowance
• Company Shuttle Service
• Annual Bonus
• Annual Salary Increment
• Performance-Based Incentives: Monthly increments
• Overtime Pay
• Shift Allowance
• Prescription Reimbursement
• Employee Purchase Program
• Group Purchase Program
• Annual Company Trip
• Sports and Recreational Activities
• New Year Party
• Death Benefits
• Family Assistance: Financial support for births, marriages, or deaths of immediate family members
• Special Leaves
• Ordination Leave
• Annual Leave
• Birthday Celebrations

Biolab Co., Ltd.

625 Moo4 BangPoo Industrial Estate,

Soi 7A, Praksa, Muang,

Samutrprakarn 10280, Thailand

Working Location: Asoke Tower (MRT Phetchaburi, BTS Asoke)

Working Day: Monday - Friday

Weare looking for a dynamic KOL Specialist to join our growing team and lead exciting skin care campaigns across major platforms like TikTok, Instagram, YouTube, and more. If you're ready to make an impact, we want to hear from you

Key Responsibilities:

• Strategic Planning & Execution: Create targeted marketing promotion plans based on product demand. Identify and partner with influential KOLs across platforms like YouTube, TikTok, Instagram, and others to enhance the GMEELAN brand presence.
• Content Creation & Guidance: Lead KOLs through the entire content creation process— from brainstorming ideas and video production to editing, reviewing, and finalizing content for upload.
• Data-Driven Optimization: Monitor and analyze the performance of influencer campaigns. Review data, measure success, and adjust strategies to ensure maximum reach and engagement.

What We're Looking For:

• Social Media Expertise: Minimum of 1 year of experience working with platforms such as TikTok, Instagram, YouTube, and Facebook.
• Passion for Digital Marketing: You live and breathe social media, staying ahead of trends and passionate about influencer marketing.
• Creative & Analytical: You have a creative mindset but also know how to dive into data to optimize results and improve campaigns.
• Strong Communication Skills: Excellent verbal and written communication skills, with the ability to collaborate with international teams.
• Basic English Proficiency: Ability to understand, speak, read, and write in English to effectively communicate with colleagues and KOLs globally.

If you are interested, please submit your Resume (English) with your recent photo, present salary and expected salary to us via Apply Now

Need more info please direct contact to: K.First /

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

Working Location: Asoke Tower (MRT Phetchaburi, BTS Asoke)

Working Day: Monday - Friday

Weare looking for a dynamic KOL Specialist to join our growing team and lead exciting skin care campaigns across major platforms like TikTok, Instagram, YouTube, and more. If you're ready to make an impact, we want to hear from you

Key Responsibilities:

• Strategic Planning & Execution: Create targeted marketing promotion plans based on product demand. Identify and partner with influential KOLs across platforms like YouTube, TikTok, Instagram, and others to enhance the GMEELAN brand presence.
• Content Creation & Guidance: Lead KOLs through the entire content creation process— from brainstorming ideas and video production to editing, reviewing, and finalizing content for upload.
• Data-Driven Optimization: Monitor and analyze the performance of influencer campaigns. Review data, measure success, and adjust strategies to ensure maximum reach and engagement.

What We're Looking For:

• Social Media Expertise: Minimum of 1 year of experience working with platforms such as TikTok, Instagram, YouTube, and Facebook.
• Passion for Digital Marketing: You live and breathe social media, staying ahead of trends and passionate about influencer marketing.
• Creative & Analytical: You have a creative mindset but also know how to dive into data to optimize results and improve campaigns.
• Strong Communication Skills: Excellent verbal and written communication skills, with the ability to collaborate with international teams.
• Basic English Proficiency: Ability to understand, speak, read, and write in English to effectively communicate with colleagues and KOLs globally.

If you are interested, please submit your Resume (English) with your recent photo, present salary and expected salary to us via Apply Now

Need more info please direct contact to: K.First /

Company Description
At Dr Reddy's "Good Health Can't Wait"
By joining Dr Reddy's, you will contribute to making the breakthroughs of tomorrow a reality today From making medicines more affordable to discovering innovative treatment options to satisfy unmet medical needs, we are dedicated to helping people lead longer and healthier lives. We are seeking dynamic and energetic individuals ready to inspire, ready to make a difference for
their
community and
every
community.

Job Description
Senior Regulatory Affairs Specialist will oversee the preparation and submission of regulatory dossiers, ensuring compliance and timely approvals. This role involves strategic regulatory planning, cross-functional collaboration and risk assessment across product lifecycle management, quality management and pharmacovigilance. Senior Specialist will provide guidance on complex regulatory challenges, drive process improvements and support audits, ensuring adherence to local and international regulatory frameworks.

Roles and Responsibilities:

• Lead the preparation and submission of the regulatory dossier, ensuring accuracy and efficiency
• Develop and execute regulatory strategies for new submissions, variations, renewals, and post-approval commitments.
• Drive regulatory compliance through proactive monitoring and risk mitigation strategies.
• Mentor and provide oversight to junior regulatory specialists, ensuring alignment with best practices.
• Actively involve in diligence of in house and partner products in every step of the product registration process until the final approval
• Review and approve artworks, prescribing information, and labelling for regulatory consistency.
• Engage with industry associations to stay ahead of regulatory changes and advocate for policy improvements.
• Lead the development and refinement of SOPs (Standard Operating Procedures) to optimize regulatory processes.
• Oversee quality management activities, including audits, risk assessments, deviations, and CAPA implementation.
• Manage pharmacovigilance operations, including adverse event reporting and compliance.
• Manage and actively involve in execution of local bio equivalence studies (import license application, LPI no. generation)
• Liaise with cross-functional teams to ensure seamless regulatory execution, including medical, commercial, and supply chain teams.
• Represent the organization in regulatory discussions with authorities and external partners.

Qualifications
Educational qualification:
A Bachelor of Pharmacy or Industrial Pharmacy or Pharm D; Pharmacy professional license holder

Minimum work experience:
5-7 years of experience in regulatory affairs, preferably with QA (Quality Assurance) and PV (Pharmacovigilance) experience

Skills & attributes:

• Good knowledge of local FDA guidelines.
• Experience with docubridge e-ctd software
• Proficiency in spoken and written English.
• Proficiency in using a computer and its applications, specifically Google Applications and MS Excel.
• Excellent interpersonal and communication skills.
• Attention to detail and the ability to multi-task and meet strict deadlines.

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