Career
WANT TO MAKE A DIFFERENCE IN SOMEONE ELSE’S LIFE? JOIN US!

With a team of over 30 people from 10 countries across 3 continents, Moleac has brought to the market the first drug that addresses gaps in pharmacological modalities. Combined with rehabilitation programmes, we offer new hopes to patients to cope with their disabilities. Join us for a life changing career!

Current Openings Here Under:

  • Medical Sales Specialist
    Medical Sales Specialist
  • Singapore
  • Product Executive
    Product Executive
  • Singapore
  • Pharmaceutical Development Engineer
    Pharmaceutical Development Engineer
  • Singapore
  • Senior Regulatory Affairs Specialist
    Senior Regulatory Affairs Specialist
  • Singapore
Medical Sales Specialist

Company And Products Description

Moleac is an internationally recognized pharmaceutical company based in Singapore focused on empowering patients affected by neurological conditions and brain injuries. Our primary mission is
to offer innovative solutions that complement existing therapies, targeting diseases with critical unmet needs.

At Moleac, we specialize in developing natural products derived from Traditional Chinese Medicine, addressing health challenges related to the Central Nervous System. Our flagship product, NeuroAiD, has already gained widespread recognition and is currently available in over 30 countries, benefiting more than 40,000 patients annually.

Looking ahead, Moleac envisions a future of continuous growth and advancement. Our strategic plans include expanding the range of indications for our existing products, reaching out to new markets globally, and introducing new therapies through the launch of new products. By doing so, we want to make a lasting impact on the lives of patients worldwide.

To meet our challenges, we are currently looking for Medical Sales Specialist to accelerate the sales in Singapore.

What You Will Do:

Lead and drive independent sales growth in Singapore
> Develop and maintain long-term relationships with customers, including doctors, medical specialists, and KOLs, while also fostering new connections.
> Do clinical and scientific detailing to doctors, opening and growing new accounts
> Regularly going into the field, meeting with customers, and consistently following up the accounts
> Develop and execute strategic sales plans, weekly field visits plan and daily visits to clinics, KOLs and potential accounts to achieve company sales targets
> Work closely with the Sales Supervisor on sales plan to achieve or exceed the sales targets set by the Management
> Provide weekly sales reports and updates to the management team, detailing progress, challenges, and opportunities
> Participate in exhibitions and conferences to represent Moleac, contributing to the expansion of brand awareness in Singapore.

What We Are Looking For:

> Academic degree in Life or Pharmaceutical Science;
> Must have at least 1-2 years pharmaceutical field sales experience in Singapore healthcare system including hospitals, clinics and healthcare centres
> Must have a solid experience in meeting with healthcare professionals and do product detailing and promotion
> Proven track record of achievement of sales and market growth in Singapore
> Result-driven with a focus on achieving sales targets
> Having prior network or relationship with healthcare professionals in Singapore is a plus
> Excellent communication skills, including comfort and proficiency in talking with doctors;
> Ability to work independently and autonomously;

If you believe you are a suitable candidate for this position, please send your CV and a cover letter (detailing your interest for the position, availabilities and expectations) to [email protected].

Product Executive

Overall Purpose of the Job

The Product Executive is primarily responsible for supporting commercial performance and company brand equity by developing new marketing campaign materials based on new data and ensuring adequate training for staff and affiliates/partners. This role also includes significant support for medical societies.

Job Profile

The Product Executive is responsible for the following key areas:
– Developing new promotional materials based on new data.
– Driving the implementation of the global campaign into both global and market-specific localized campaigns.
– Ensuring proper appropriation of materials, appropriate training levels within the organization, and collecting feedback.
– Supporting the marketing team to build the company’s brand and marketing strategies to drive revenue generation.
– Planning appropriate internal meetings to ensure strategy, key messages, and tactics are understood and delivered.
– Conducting market analysis to drive successful marketing strategies.
– Ensuring the effectiveness of marketing/promotional materials, Key Account Managers (KAMs), and stakeholder engagement activities are researched, with measures in place to monitor effectiveness and return on investment.
– Developing key dashboards for each asset to track progress and highlight issues.
– Building and maintaining relationships with medical societies and providing continuous support for their projects.
– Maintaining and further building relationships with local and international key opinion leaders.

Job Requirements

We are looking for a highly motivated candidate, passionate about Pharma-marketing who can:
– Develop scientific promotional materials and provide a high standard of training.
– Deliver Marketing Brand and Execution Plan outcomes and key performance indicators in line with Brand Strategies.

Basic Qualifications

– Preferably a degree in Pharmacy/Science.
– Scientific acumen.
– Strong analytical and project management skills.

Competencies Required

– Excellent command of English (oral and written) for developing material is an absolute must.
– Ability to speak another language relevant to the client base will be an advantage.
– Success in partnering and working with other functions such as Medical, Sales, and Regulatory.
– Ability to work in a team and independently with minimal supervision, self-motivated, disciplined, and proactive.
– Creativity with good negotiation and influencing skills.
– Strong facilitation and presentation skills to both internal and external stakeholders.
– Ability to identify and resolve customer queries and problems immediately and maintain good relationships with Healthcare Professionals.
– Excellent time-management skills with the ability to successfully manage numerous projects simultaneously and drive change.
– Demonstrated ability to work in a fast-paced environment while remaining flexible and adaptable to rapidly changing priorities.
– Ability to work in a multilingual and multicultural environment where collaboration is a key value.
– Strong analytical skills, with the ability to set and closely monitor KPIs.
– Ability to prioritize workload and manage multiple tasks simultaneously.
– Strict attention to detail, ability to work well under pressure, and meet tight deadlines.
– Dynamic, ambitious, with a strong desire to succeed.

What’s on Offer

You will be part of a dynamic, multicultural, and fast-paced environment. Moleac has shown stable and rapid growth since 2006, pursuing geographical expansion while investing heavily in research and development. Moleac values young talents and provides real opportunities to take on great responsibilities to sustain its continuous growth. In addition to your package (Basic + attractive bonus scheme + medical cover), you will benefit from regular training and have the opportunity to develop your skills and leadership throughout your career with the Group.

Application Process

If you believe you are a suitable candidate for this position, please send your CV and a cover letter (detailing your interest in the position, availability, last drawn salary, and salary expectations) to [email protected].

Incomplete applications will not be reviewed.

Note: Only shortlisted candidates will be contacted.

Pharmaceutical Development Engineer
Summary of Job

Department: CMC & Supply Chain
Location: Singapore
Working as a SME (Subject Matter Expert) that will be involved in manufacturing process and quality control analytical methods improvement, technical support for manufacturing activities internally, network and collaborate with academia externally.

ESSENTIAL DUTIES & RESPONSIBILITIES
CMC Support

– Compile, analyse and present chemical, manufacturing control, biological testing related data in a concise manner for review with the project team and decision;
– Develop improved understanding of the process and analytical techniques in building CMC dossier to support discussion with authorities;
– Responsible for compiling and preparing quarterly reports of CMC developments for all projects;
– Source and select new external CRO/vendor/suppliers, participate in qualification of selected CRO/vendor/suppliers, in collaboration with QA;
– Provide technical support for clinical and non-clinical activities;
– Provide technical support for patent filing

QC Support

– Perform timely batch release of raw materials and finished product to ensure commercial order fulfilment;
– Ensures timely update of manufacturing master batch records to ensure GMP compliance;
– To be on site to observe the production to ensure the contract manufacturer to produce Moleac’s products as per requirement if needed;
– Investigate deviations, propose and execute strategies to resolve quality investigations;
– In collaboration with QA, perform investigation for customer complaint;
– Develop and maintain relevant department SOPs

Qualifications

– Degree/Master/PhD with a minimum of 3 years of experience in pharmaceutics, chemical engineering, chemistry, or allied disciplines. Exceptional candidates with less experience will also be considered.
– Solid knowledge in modern analytic, various spectroscopic and chromatographic analytical method is required.
– Previous experience working in a cGMP environment with in-depth knowledge of cGMP and relevant quality management systems will be an added advantage.
– Excellent oral and written communication skills. Knowledge of Chinese/Mandarin is essential to liaise with external CMOs and partners.
– Previous experience within CMO, or CDMO preferred.
– Ability to prioritize and manage multiple projects and activities while meeting tight deadlines
– Proven ability to think critically, proactive in problem-solving and able to independently manage timelines and priorities.
– The candidate will be required to travel on a periodic basis.

If you believe you are a suitable candidate for this position, please send your CV and a cover letter (detailing your interest for the position, availabilities and expectations) to [email protected].

Senior Regulatory Affairs Specialist
Summary of Job

The Senior Regulatory Affairs (RA) Specialist contributes to all regulatory functions for Moleac products such as obtaining marketing authorisations and product life-cycle management for the global market, and assigned projects.

The candidate demonstrates consistent and excellent interpersonal and communication skills along with ability to thinking critically, problem-solve and collaborate effectively with internal stakeholders.

Key Responsibilities

– Prepare and review registration/ variations dossiers for submission to regulatory authorities, ensuring scientific rigour, consistency and accuracy of product information, alongside good documentation practice.
– Coordinate with partners and regulatory consultants abroad to support overseas registration, in accordance to company strategy and timeline.
– Collaborate with stakeholders and contribute actively to all aspects of product life cycle management, ensuring compliance to applicable regulatory and quality requirements and continuity in commercialisation.
– Maintain and build on existing database of applicable health product regulations, standards, and guidance documents, interpreting emerging regulations and developments to assess impact on products.
– Review promotional material developed for commercial activities to ensure compliance to applicable regulatory guidelines.
– Participate in local and overseas regulatory inspections and internal audits when applicable.
– Develop and maintain effective relations with local authorities and industry associations Provide regulatory inputs and support to clinical trials and ethics committee submission.
– Assist in GDP and relevant quality assurance matters.
– Lead and support project groups to ensure business objectives are met
– Assist in formulate regulatory strategy that meets registration timeline and business objectives
– Provide guidance to the junior RA staff and interns to help build their competency

Personal Attributes/ Core Competencies

– Highly-organised and self-disciplined.
– Resourceful, with analytical and problem-solving skills.
– Able to prioritize and work well in fast-paced environment.
– A team player with excellent interpersonal skills.
– Experienced in guiding interns or junior team member
– Driven and result focus, able to coordinate with internal and external stakeholder effect to complete task on time
– Flexible and able to pivot quickly when business objective changes
– Proficiency in English (both written and spoken). Additional language such as Mandarin is a strong plus to liaise with external CMOs and partners.

Qualifications

– Degree in life sciences or pharmacy, with min. 3 – 5 years of relevant work experience. Prior Regulatory experience in regional setting would be advantageous
– Knowledge in international regulatory guidelines such as ICH, ASEAN, USFDA, EU etc. Regulatory experience with food supplement/ herbal medicine in Europe, North America or Asia Pacific would be advantageous.
– Good understanding in GMP, GDP and relevant quality management systems desirable.

If you believe you are a suitable candidate for this position, please send your CV and a cover letter (detailing your interest for the position, availabilities and expectations) to [email protected].