Careers
We offer an environment that nurtures people to strive for excellence. We pride ourselves in our immaculate process of mentoring, coaching and training. We consider our employees as our best assets and as partners who work synergistically for the growth of the organization. Our work culture is one that values each person’s ideas and contributions. We encourage our employees to develop holistically by providing incentives for self-growth in areas as diverse as sports and creative arts. Practical ideas for process improvements are rewarded through cash rewards or gift coupons.
We are passionate about our work but we play hard too!
Please apply if you want to join our vibrant team.
Vacancies
WE ARE HIRING!
REGULATORY AFFAIRS CONSULTANTS/QMS CONSULTANTS/SCIENTIFICWRITERS
Are you a passionate and detail-oriented regulatory
affairs professional with a fire for innovation in
healthcare ?
We are a rising star in regulatory and QA consulting and training.We seek
experienced professionals from the regulatory ,QA,and medical/technical
writing domains to join our dynamic team and play a privotal role in ensuring
that our work effectively and efficientl achieves customers' goals.
This is an office-based job.Only those willing to work from our vadodara,
Gujarat office may apply.
These positions are open only to experienced professionals with around 3-6
years of work experience.
We perfer people working in the manufacturing sector who to switch
to a consultant’s role.
IN THIS ROLE, YOU WILL:
Provide strategic regulatory guidance and support to customers who are primarily manufactuers of medical devices and IVD devices
Manage the preparation and submission of regulatory documentation for local and international markets
Liaise effectively with regulatory agencies and address queries.
TO BE SUCCESS, YOU MUST HAVE THE FOLLOWING QUALIFICATIONS AND COMPETENCIES:
- Graduate or post graduate in an engineering discipline (electronics, electrical, mechanical, biomedical)or
pharmacy. - 3-6 years of expericence in regulatory affairs,QA or medical writing within the healthcare sector,
preferably from medical device or IVD device manufacturing companies. - Proven experience preparing and submitting regulatory filing, implementing quality management ststem,
and preparing clinical evaluation or clinical trial documents. - Strong understanding of relevant regulatory requirements
- A desire to continuously learn and skill oneself
- Excellent written communication skill in english, without the use of al tools
- Good analytical and problem-solving skill.
- Ability to manage multiple priorities and work independently.
- Stay current on evolving regulations and industry trends.
- Be able to collaborate with cross-functional team
WE OFFER:
- A competitive salary and benefits package.
- Opportunity to continuously learn and gain skills
- The opportunity to work on innovative products
- A collaborative and free work environment.
- A chance to play a key role in shaping the future of healthcare.
We are an equal-opportunity employer and value diversity at our company.
READY TO MAKE YOUR MARK?
Work with Us
Careers
You can contact us on the following sources
Say Hi!
contact@alceonconsulting.com
Let's Talk
+91 9925023428
