Unilever looking to hire an Assistant Manager – RegulatoryAffairs in the team based in Bangalore/Mumbai/Gurgaon. We are providing the details of the MSc Chemistry MPharm vacancy here. Apply now for the MSc Chemistry MPharm vacancy at Unilever.
Job ID: R-68456
Job role – Assistant Manager Regulatory Affairs, South Asia
Location: Mumbai, Maharashtra
MAIN JOB PURPOSE:
- Regulatory Affairs (RA) is a global capability in Unilever R&D that promotes science and evidence-based thinking in development of standards, regulations, and policies. The RA team ensures Unilever’s freedom to operate and enables landing safe and sustainable innovative products into markets, to serve our consumers better.
- South Asia, is one of the biggest markets for Unilever, witnessing a transformation of regulatory environment and an increasing commitment to the deliver on the SDGs. For Unilever this represents an opportunity to collaborate with the regulators, industry associations and stakeholders to leverage our global capabilities and help shape new technical standards, regulations, and policies.
- Based within its global R&D centre at Bangalore, India, Unilever S. Asia is looking for Assistant Manager Regulatory Affairs (Operations & Program) – S. Asia
- The employee will work closely with Head Regulatory Affairs (RA) S. Asia and with RA colleagues across Business Groups and Business Units in S. Asia region.
The primary objective/ deliverables of MSc Chemistry MPharm vacancy:
- ensure seamless coordination of various RA initiatives/ programs ongoing in S. Asia and as relevant, globally
- research standards, regulations, and policies across S. Asia and globally, and collaborating with R&D and other relevant stakeholders, prepare compelling position papers for changes and improvements
- work with relevant industry associations, build momentum and bring actions that result in change
- plan and coordinate S. Asia RA team meetings and events, seminars, and institute an annual calendar for the team/ function
- Participate in departmental budgeting, tracking spends and resourcing / prioritization
- draft agendas, take minutes and follow up on actions with the team members
- meet, liaise with, and discuss important regulatory matters with government officials
- maintain current knowledge of relevant regulations, including proposed and final rules
Skills and Competencies:
- Strong understanding of safety, quality, sustainability, and regulatory aspects of consumer goods
- Strong bias for action
- Penchant for science communication and visualization
- Digital and social media savvy
- Keen eye, meticulous record keeping and attention to detail
- A collaborator who thrives on working together with different teams
- A strong business mindset focusing on what is needed to drive impact and business results
- Ability to understand relevant technical-scientific topics and to translate them for stakeholders
- Must have excellent interpersonal, communication and collaboration skills as required for internal and external networking.
- Open, global mindset characterized by positivity, flexibility, and adaptability with agile thinking
- Strong research and intelligence gathering background enabling collation of information and research for use in issue management and/or strategy development for public policy and advocacy
- The position involves frequent travel for meetings, conferences/events. A willingness to travel is therefore a pre-requisite
- Proactivity to accomplish goals, complete tasks and assignments
- Positive and optimist about the world and believes that small everyday actions can bring big change
Qualified science/ technology post-graduate with outstanding academic credentials. M. Pharm/ M. Tech (Food Tech.)/ M. Sc. (Lifesciences/ Chemistry). Qualifications in public policy/ law will be an added advantage
Experience:
- Not less than 3 years in a similar capacity across consumer goods, pharma, medical devices
- Track record of the following will be preferred:
- working in/ contribution to development of standards and regulations
- having planned/ organized scientific/ technical events
- writing technical papers/ article
- building and developing networks/coalitions around issues
Hello friends, we are attaching some of the expected interview questions and answer here. Please prepare for the interview for the MSc Chemistry MPharm vacancy using the same. All the best!!!
Question: Can you share your experience in working with regulatory standards and policies in the consumer goods or related industries?
Answer: Certainly. Over the past three years, I have been actively involved in dealing with regulatory affairs in the consumer goods industry. This includes working closely with regulatory standards and policies, ensuring compliance, and preparing position papers to advocate for changes and improvements. I have also collaborated with relevant industry associations to drive actions that align with regulatory requirements.
Question: The role emphasizes the need for excellent interpersonal and collaboration skills. Can you provide an example of a challenging situation where you effectively collaborated with different teams to achieve a common regulatory objective?
Answer: In a previous role, we were faced with a complex regulatory challenge that required cross-functional collaboration. Our team needed to align with R&D, marketing, and legal departments to meet a critical compliance deadline. Through effective communication and collaboration, we organized regular meetings, shared updates, and addressed concerns proactively. This collaborative effort resulted in successful compliance and strengthened our working relationships.
Question: The job requires research and intelligence gathering for public policy and advocacy. How have you demonstrated these skills in your previous experiences?
Answer: In my prior roles, I have been responsible for researching and gathering relevant information to support issue management and strategy development for public policy and advocacy. I have written technical papers and articles that highlighted the impact of regulatory changes on our industry. Additionally, I actively participated in industry events, conferences, and seminars to stay informed about emerging regulatory trends.
Question: The position involves frequent travel for meetings and events. How do you ensure you manage travel efficiently and maintain productivity while on the go?
Answer: I understand that frequent travel is a part of the job and I am fully prepared to manage it efficiently. To ensure productivity, I plan my travel in advance, optimize schedules, and make the best use of travel time for tasks like reviewing documents or preparing for meetings. I am comfortable using digital and social media tools to stay connected with the team and stakeholders, even while on the move.
Question: The role requires a keen eye for detail and meticulous record-keeping. How do you ensure accuracy and precision in your work?
Answer: Attention to detail has always been a priority for me in my work. I double-check information, review documents thoroughly, and maintain meticulous records of all regulatory activities and updates. I also believe in seeking feedback from colleagues and supervisors to ensure the highest level of accuracy in my work.
Question: Can you tell us about your experience in organizing scientific or technical events?
Answer: In my previous role, I was responsible for planning and organizing several scientific symposiums and technical workshops. These events brought together experts from different fields to discuss emerging trends and regulatory challenges. I managed event logistics, coordinated with speakers and attendees, and ensured the smooth execution of the events, resulting in positive feedback from participants.
